Difference between revisions of "Team:Valencia UPV/Notebook"

Latest revision as of 15:52, 18 September 2015

Valencia UPV iGEM 2015

Protocols

Here we present you all the procedures we did to develop our project. On this page you can find the general protocols. If preferred, you can go directly to the dialy Notebook, the experiments on Nicotiana or the protoplasts experiments by pressing in the buttons above or below (after protocols). We hope you enjoy reading our incredible journey!

Constructions protocol

2. Ligation in pUPD2:

The ligations have a total volume of 10 µl. All the parts were mixed together in an eppendorf of 0.2ml. The eppendorf was put in the thermocycler with the programs GB or GG, the differences between them are number of cycles. Explain the cycles!

*The cells with the asterisk are the ones that are going to be written down and specified in the lab-book. The others cells are constant unless we indicate it specifically on the lab-book.

DNA; pUPD2

1 µl DNA fragment

1 µl pUPD2

1.2 µl buffer ligase

1.2 µl BSA (10x)

1 µl BsmbI

1 µl T4 ligase

5,6 µl H₂O

8. Ligation in α or Ω:

DNA1;pUPD2+DNA2;pUPD2 ; α	DNA1; α1+DNA2; α2; Ω
1 µl DNA1; pUPD2	1 µl DNA1; α1
1 µl DNA2; pUPD2	1 µl DNA2; α2
1 µl α	1 µl Ω
1.2 µl buffer ligase	1.2 µl buffer ligase
1.2 µl BSA	1.2 µl BSA
1 µl T4 ligase	1 µl T4 ligase
1 µl BsaI	1 µl BsmbI
4.6 µl H₂O	4.6 µl H₂O

3a. Transformation:

In order to transform the DNA construction the electroporation method was used.

The method followed is common for E. coli and Agrobacterium. The electroporation cuvette was put in ice 10 minutes before inserting the cells.

Frozen cells were taken out of the -80ºC freezer, and they were put immediately into ice.

1-2 µl of the ligation were taken and added carefully to the electrocompetent cells.

60 µl of the mix were taken and put into an electroporation cuvette making sure that there were no bubbles.

The cuvette was dried and put in the electroporator, making sure that it did not do a spark. In that case, the process did not work and must be repeated.

The voltage is 1500V for E. coli and 1440V for Agrobacterium.

Then with 300 µl of medium the electroporated cells were taken and put into an Eppendorf, letting them grow in the shaker.

SOC medium was used for E.Coli and they were put at 37ºC for 1h.

LB medium was used for Agrobacterium and they were grown for 2h at 27ºC.

3b. Petri dish culture:

Depending on the plasmid with which the bacteria was transfected, agar dishes with the specific antibiotic were needed to make the petri dishes cultures.

E. coli-pUPD2 plasmids: chloramphenicol.
E. coli-Alpha 1 and 2: kanamycin.
E. coli-Omega 1 and 2: streptomycin
Agrobacterium: rifampicin + the specific one for each construction.

The procedure was made in the laminar flux cabinet. The spread plate method is done with 50-40 µl of the bacteria culture that is in the eppendorf. It was spread with the glass dipstick. After that the plates were put for 16h approximately in 37ºC for E. coli and 32h at 28ºC for Agrobacterium.

4. Liquid culture:

For Escherichia coli:

The mix was grown 16h at 37ºC in the shaker.

For Agrobacterium tumefaciens:

The mix was grown 32h at 28ºC in the shaker.

5. Minipreps:

In order to do the minipreps -extraction of the plasmids out of E. coli the protocol of the Omega kit (Plasmid DNA Mini Kit I Spin Protocol) was used. The steps to do it are:

1. Centrifuge at 10.000xg for 1minute at room temperature the liquid medium with the growed bacteria.

2. Decant or aspirate and discard the culture media.

3. Add 250 µl SolutionI/RNase A. Vortex or pipet up and down to mix thoroughly. Complete resuspension of cell pellet is vital for obtaining goo yields.

4. Tranfer suspension into a new 1.5mL microcentrifuge tube.

5. Add 250 µl Solutions II. Invert and gently rotate the tube several times to obtain a clear lysiate. A 2-3 minute incubation may be necessary.

6. Add 350 µl Solution III. Inmediately invert several times until a flocculent white precipitate forms.

7. Centrifuge at maximum speed (>13.000xg) for 10 minutes. Acompact white pellet will form. Promptly preceed to the next step.

8. Insert a HiBind DNA Mini Column into a 2 mL Collection tube.

9. Transfer the cleared supernatant from Step 8 CAREFULLY aspirating it into the HiBind DNA Mini Column. Be careful not to disturb the pellet and that mo cellular debris is transferred the the HiBind DNA Mini Column.

10. Centrifuge at maximum speed for 1 minute.

11. Discard the filtrate and reuse the collection tube.

12. Add 500 µl HBC Buffer.

13. Centrifuge at maximum speed for 1 minute.

14. Discard the filtrate and reuse collection tube.

15. Add 700 µl DNA Wash Buffer .

16. Centrifuge at maximum speed for 1 minute.

17. Discard the filtrate and reuse the collection tube.

18. Centrifuge the empty HiBind DNA Mini Column for 2 minutes at maximum speed to dry the column.

19. Transfer the HiBind DNA Mini Column to a clean 1.5 mL microcentrifuge tube.

20. Add 30-100 µl Elution Buffer or sterile deionized water directly to the center of the column membrane.

21. Let sit at room temperature for 1 minute.

22. Centrifuge at maximum speed fot 1 minute.

6a. Digestion:

After doing the miniprep the DNA was obtained. The next components were mixed up in a 200 µl eppendorf. After the mix was done it stayed at 37ºC, 1h.

1 µl of the DNA

1 µl specific buffer

0.5 µl of the specific enzyme

7.5 µl of H₂O

1 µl of loading buffer is needed for each 5 µl of the digestion mix, so they were added 2 µl of loadding buffer (6x).

These are the specific enzymes and buffers for each type of plasmid.

Plasmid	Enzyme	Buffer
pUPD2	Not I	Orange
Alpha	EcoRI	Specific
Omega	BamHI	Specific

The plasmids can also be cut with other enzymes if it is necessary to check the construction.

6b. Gel:

The gel was made with buffer + dilution 1:1000 of ethidium bromide and a proportion of 0.1% of agarose.

The small gels had 40ml of buffer + 0.4 µl of ethidium bromide and 0.4g of agarose.

After waiting 1h to let the gel cool down, the ladders of 100bp and 1kbp are put one on each side of the gel, and the digestions in between the ladders.

The voltage to apply is 120V.

It was written in a table the DNA fragments obtained and the words “ok “ or “no” depending on if the results are correct or not. Example:

DNA1	DNA2 C1	DNA2 C2	DNA4
ok	no	no	ok

7. Sequence:

To check if the plasmid obtained has the proper construction, a Sanger sequencing was made.

The IMBCP has its own sequencing service.

Agroinfiltration protocol

The agroinfiltration is a process that consist of introducing Agrobacterium tumefaciens into a leaf plant by is underside. Agrobacterium tumefaciens is a bacteria that causes the formation of tumours in some plant species like Nicotiana benthamiana, the one that we are working on. This bacteria carried the plasmid that have the DNA construction we want to test and as it infects the cell plants produce a transitory expression of our DNA piece.

So to start the process of the agroinfiltration first of all we have to grow Agrobacterium in liquid culture two days, then refresh two times this first culture taking 5µl of the previous culture. The refresh cultures are only one day incubating at 28ºC. After this starts the procedure:

1. Centrifuge the Agrobacteriumcultures 10min at 3000rpm.

2. While doing this prepare the agroinfiltration solution. It is made of 10ml of MES 10x (100mM, pH 5.6) + 1ml MgCl2 (1M) + 100µl of acetosyringone solution (200mM) it is composed by 9.8mg of acetosyringone dilute with 250µl of DMSO. Add water up to 100ml.

3. Eliminate the supernatant of the cultures and then add 5ml of the agroinfiltration solution. Resuspend the bacteria and let them grow in dark in the shaker.

4. Measure the OD (optical density). To do this the Agrobacteriumculture is diluted in proportion 1:10 so it is put 900 µl of agroinfiltration solution and 100 µl of bacteria culture and then measure in the spectofotometer. Depending on the OD obtained the culture will be diluted with a quantity that gets the ODs to 0.2 (when infiltrating viral system the OD has to be 0.1).

5. The dilute bacteria is put in eppendorfs and are ready to agroinfiltrate.

Tips to agroinfiltrate:

Do the infiltration on the young leafs without rough surface.
Put the syringe with the solution that has bacteria in the undarside and gently introduce the liquid making also a bit of presure with the finger in the adaxial surface of the leaf.
Change the gloves and the syringe each time you change construction that wants to be agroinfiltrated.
Take the plants out in baches to avoid that due to de hot ambient they close their pores.

Luciferase assay protocol

Before start:

This procedure is done with the Promega; kit (Dual-Luciferase Reporter Assay System).

First of all is needed to agroinfiltrate the plant and let them for 2 o three days depending on how the experiment is raised. Normally in this days the plants are in darkness because our pieces to tests activates with different wavelegth of ligths. After two days discs are made, trying to take the maximum agroinfiltrated area without any nerve. The discs are put in the specific plate depending on in which ligth condition they need. The samples are taken during one or two days after the discs were made and inmediately the are put in liquid nitrogen and the storage in the -80ºC fridge.

The steps to follow are:

1. The Passive lysis buffer 1x is prepared. It is used 200µl per disc of leaf. The passive lysis buffer is 5x so diluted them with destilled water, always manipulate in ice.

2. Grind the freeze sample with a machine that shake the eppendorfs that had to have previusly two little metal balls or with plastic maces.

3. Add to the eppendorf 150µl of passive lysis buffer 1x.

4. Mix it with the vortex avoiding that they melt. Do this step in cold the maximum time possible.

5. The samples are centrifuged in cold during 15min at 13200rpm.

6. A dilution 2:3 is made with the extract, to do that put in a new eppendorf 36µl of passive lyssis buffer 1x and 24µl of sample.

7. The opaque plate to use in the luminometer is taken. 40 µl of Luciferase is added in each well.

8. 10 µl of sample is added too. Wait 10min. During this time turn and configurate the luminometer.

9. The luciferase activity is mesured.

10. 40 µl/sample +1extra of Dual Glo (1x) was prepared . The sustrate is at 50x and it is at –20ºC, the buffer to dilute it is in the fridge.

11. After the first masure is done add to the wells 40 µl of Dual Glo, let it 10 min and measure the Renilla.

12. Take the data obtained and analyze it.

Things to keep in mind for the next experiment:

The luminimeter (machine to measure the luminescence) has to be ready before start adding the reactants to the samples because it needs 10min to be ready.
Set the timer (10min) with the first sample of luciferase and add the reactant to the other samples as quick as possible.

Western blot protocol

DAY 1

PROTEIN EXTRACTION

1. Harvest agroinfiltrated leaves. Grind the harvested material in liquid N2. You can store ground tissue at -80ºC.

2. Weigh around 100 mg of ground tissue in a 1.5 ml tube. Keep sample frozen!

3. Add 3 vol. ice-cold extraction buffer to each sample (300 µl buffer/100 mg tissue).

4. Mix thoroughly by vortexing for a few seconds. Transfer samples to ice. Repeat vortexing a few times (cooling the sample in between) till sample is completely thaw.

5. Centrifuge the extract for 15’, at > 12000xg, 4ºC.

6. Transfer the supernatant to a fresh 1.5 ml tube. Samples should be kept cold at all times, work on ice!

SDS-PAGE

1. Sample Mix Preparation ( for 10 µl final volume, scale up as necessary):

Protein extract	1 to 6.5 µl
NuPAGE LDS Sample buffer (x4)	2.5 µl
NuPAGE LDS reducing agent (x10)	1 µl (use only for reducing conditions)
Ultrapure H₂O	0 to 5.5 µl

Mix by vortexing. Heat at 72ºC^(*) for 10’. Spin briefly to collect everything at the bottom of the tube. Keep samples on ice.

2. Assembling the gel and loading the samples:

Prepare 800 ml MES SDS 1x running buffer

20x MES MES SDS running buffer	40 ml
Distilled H₂O	760 ml

Set aside 200 ml of 1x running buffer. Add 500 µl of NuPAGE antioxidant (only for reducing conditions). Mix by inversion.

Take one 10% Bis-Tris NuPAGE gel out of the plastic bag and rinse with distilled H₂O. Peel off the white tape at the bottom of the gel.

Pull out the comb.
Insert the gel in the sure lock gel. The shorter well side of the cassettes facing inwards. Lock the gel tension wedge.
Fill the upper buffer chamber with the 200 ml of 1x running buffer with antioxidant. Fill the lower buffer chamber with remaining 600 ml of 1x running buffer.

To load the samples: insert the tip into the well and slowly pipet the sample into it.

3. Running the gel:

Running conditions: 200 V, 40 min

PROTEIN TRANSFER

1. Preparing for transfer:

Cut 1 piece of Hybond-P PVDF membrane and 2 pieces of whatman paper of the same size of the gel (8 x 7 cm).
Prepare 500 ml of Transfer buffer:

Transfer buffer (x20)	25 ml
Methanol	50 ml
H₂O	375 ml

Soak 5 blotting pads in transfer buffer. Remove air bubbles by squeezing the blotting pads while they are submerged in buffer (this step is important because air bubbles may block the transfer of proteins).
Pre-wet the PVDF membrane for 10’’ in methanol. Wash in distilled water for 5’. Equilibrate in transfer buffer for at least 10’ before blotting. (Everything is done without agitation).
Wathman paper: soak briefly in transfer buffer immediately before using.

Lay the gel on the bench allowing one edge to hang 1 cm over the side. Insert the gel-knife into the gap between the gel plates and push up and down gently to break the bonds that hold the plates together. When all the bonds are broken separate the two plates and throw away the one without the gel.
Cut the wells with the gel-knife.
Place a piece of pre-soaked whatman paper on top of the gel. Keep the filter paper saturated with transfer buffer and remove all trapped air bubbles by gently rolling a glass pipette over the surface.
Turn the plate over so that the gel and whatman paper are facing downwards over your hand or over a piece of parafilm on the bench.
Remove the gel from the plate: use the gel knife to carefully loosen the bottom of the gel so that it peels away from the plate.

3. Transferring the gel:

Wet the surface of the gel with transfer buffer and place a pre-soaked membrane on top of the gel. Make a small cut on one corner of the membrane to mark the orientation. Remove air bubbles by rolling a glass pipette over the membrane surface.
Place a pre-soaked whatman paper on top of the membrane. Remove air bubbles.
Place 2 soaked blotting pads into the Xcell II Blot Module. Place the paper-gel-membrane-paper sandwich on top of the blotting pads.
Add another 3 pre-soaked blotting pad on top of the sandwich.
Place the blot module in the buffer chamber. Lock the gel tension wedge into place.
Fill the blot module with transfer buffer until the gel-membrane sandwich is covered in buffer (do not fill all the way to the top as this generates extra conductivity and heat).
Fill the outer buffer chamber with ˜ 650 ml deionized water.
Running conditions: 30V for 2h

BLOCKING THE MEMBRANE

1. Prepare 50 ml of blocking solution.

2% ECL Advance Blocking Agent in PBS-T (pH 7.5):

1 g blocking agent
50 ml PBS (1x)
50 µl Tween-20

2. Take the membrane out of the blotting module and transfer it to the blocking solution (protein side up, work always this way from now on). Leave o/n at 4ºC.

DAY 2

DETECTION

1. Prepare 2 L of wash buffer (PBS-0.1% Tween (pH 7.5))

200 ml PBS 5x (pH 7.5)
800 ml distilled H₂O
1 ml Tween 20

3. Prepare 10 ml of antibody diluent (2% ECL Advance blocking agent in PBS-0.1%Tween) for each antibody you are going to use.

4. For 6x His-tag detection: dilute the Anti-His6 mouse monoclonal antibody 1:2000 in 10 ml of antibody diluent (5 µl antibody in 10 ml antibody diluent). Incubate for 1h at RT on a shaker.

For IgA detection: dilute the Anti-IgaH antibody 1:20000 in 10 ml of antibody diluent (0.5 µl antibody in 10 ml antibody diluent). Incubate for 1h at RT on a shaker. This antibody is already conjugated to HRP and does not need a secondary antibody for detection; go directly to step 8 after the 1 incubation.

5. Discard the antibody solution and wash the membrane with wash buffer:

2 x brief wash
1 x 15’ wash (RT, shaker)
3 x 5’ wash (RT, shaker)

7. Incubate the membrane with the secondary antibody for 1h at RT on a shaker.

8. Repeat step 5.

9. Take the detection reagents from the fridge and allow to equilibrate to RT before opening.

10. Mix detection solutions ECL Plus A and B in a ratio 40:1.

975 µl Sol. A + 25 µl Sol. B (enough for 1 membrane)

11. Drain the excess wash buffer from the membrane by holding the membrane gently with forceps and touching the edge against a tissue. Place the membrane protein side up on an acetate sheet. Pipette the mixed detection reagent on to the membrane.

12. Cover the membrane with another acetate sheet and gently smooth out any air bubbles, but do not apply pressure over the membrane. Dry any extra liquid with tissue.

13. Place a piece of filter paper on a X-ray film cassette (fix with tape). Drain excess of detection solution with a tissue and place the wrapped blots on top of the paper (fix with tape). Close the cassette and take to the dark room together with the autoradiography films and timer.

14. Switch on the film processor (front panel, lower right corner). Check that the temperate selector on top of the switch on button is on position 2. Turn off the light and with the red light on open the cassette and place a sheet of autoradiography film on top of the membrane (bend the lower right corner to mark the orientation). Close the cassette and expose the film for 1’. To develop the film place it on the rear feeding tray (shorter side of the film opposite to the bent corner against the feeding area to minimize the possibility that the film gets stack in the processor) and press the button next to it to start the feeding. Adjust exposure time as necessary.

Protoplasts protocol

We make protoplasts in to different ways. At first we make protoplasts with a normal Nicotiana leaf and then we try to transform the alive protoplasts. After the infiltration at vacuum we can not obtain protoplasts, we change the method. First we agroinfiltrate leafs with the desired construction, we let them 3 hours in dark and then make the protoplasts. The general steps for every preparation is:

1. Prepare the enzymatic solution. It has 5mL of Mannitol (0.8M) + 200 µl KCl (1M) + 400 µl MES (0.5M, pH 5.7) + 150ng cellulase + 40mg Macerozyme + 4.2mL H₂O. Total volume for one preparation. Put it 10min at 55ºC.

2. Take out the solution and let it cool down.

3. Add 100 µl CaCl₂ + 4 µl Beta-Mercaptoethanol + 100 µl BSA (10%).

4. Put the enzymatic solution in a petri dish and cut the leaf in very thin strips. Put quickly the cut leafs so they do not dry.

5. In darkness, do the vacuum for 30min to the petri dish with the enzymatic solution and the cut leaf. Let the leaf 3h in darkness, no agitation.

6. Swirl the plate gently. Using a 5ml pipette tip (cut off the tip first) take the liquid and filter them with a 35-75 µm nylon mesh into a 13 mL tube. To clean the mesh add before a little bit of W5 solution. Also put the leaf stripes first and then throw the enzymatic solution.

7. Add 5ml of W5 solution.

8. Centrifuge at 100xg for 1min without brake.

9. Eliminate the supernatant. Leave a small volume so that the protoplasts do not dry.

10. Add WI solution till reach the desired concentration (10⁷ protoplasts per gram).

11. Finally put into the plate wells 250 µl of W5 and 100 µl of protoplasts solution.

Solutions:

W5: NaCl (154mM) + CaCl₂ (125mM) + KCl (5mM) + MES (2mM) + 17.8ml H20. Total volume of 50ml.

WI: MES (4mM)(pH 5.7) + NaCl (154mM) + CaCl₂ (20mM).

Protoplast luciferase assay protocol

Before doing the essay the protoplasts are in a plate in the light conditions needed.

1. Take the solution with protoplasts and put it in an Eppendorf.

2. Centrifugue at 100xg for 1min.

3. Eliminate the maximum supernatant letting the protoplasts.

4. Put into liquid nitrogen and then keep it in the -80ºC fridge.

Start the essay:

5. Add to the freeze sample 100µl of Passive lysis buffer (1x).

6. Vortex the samples.

7. Let it 5min in ice.

8. Centrifuge it at 1000xg for 2min.

9. Eliminate the supernatant.

10. Take an opaque plate to measure the luciferase and put in each well 40 µl of Luciferase and 10 µl of sample, wait 10min and then measure.

11. Add to the wells 40 µl of Dual Glo (1x) and measure the renilla luminiscence.

Go to Daily notebook

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@@ Line 1: / Line 1: @@
 {{:Team:Valencia_UPV/Templates:headUPV}}
 {{:Team:Valencia_UPV/Templates:menuUPV}}
+<html>
+	<!-- Banner -->
-<html>
-			<!-- Banner -->
-				<section id="banner">
 <style>
-				#banner{background-image: url("images/overlay.png"), url("https://static.igem.org/mediawiki/2015/8/89/Valencia_upv_notebook.JPG");}
+	#banner{background-image: url("images/overlay.png"), url("https://static.igem.org/mediawiki/2015/8/89/Valencia_upv_notebook.JPG");}
-				</style>
+</style>
-					<h2 style="font-weight:bold">Notebook</h2>
+<section id="banner">
-					<p>Be patient, we are under construction</p>
+	<h2>Notebook</h2>
-					<ul class="actions">
-						<li><a href="#" class="button">Protocol</a></li>
-						<li><a href="#" class="button">Construction</a></li>
-						<li><a href="#" class="button">Experiment</a></li>
-					</ul>
-				</section>
-			<!-- Main -->
-				<!-- Main -->
-	<section id="main" class="container">
-				<div class="row">
-						<div class="12u">
-<section class="box">
-<h3 style="color:green">5 June 2015</h3>
-<p>We had 2 cultures from the last day, corresponding to other 2 colonies of ligation. </p>
+	<ul class="actions">
+<li><a href="https://2015.igem.org/Team:Valencia_UPV/Notebook#scroll1" class="button">Protocols</a></li>
+<li><a href="https://2015.igem.org/Team:Valencia_UPV/Notebook/Content#scroll1" class="button">Daily notebook</a></li>
-<p><i>Agrobacterium</i> culture of promoter less: Luciferase + Renilla </p>
+	</ul>
+</section>
-<p>Minipreps</p>
+<!-- Main -->
-<p>Digestion with BamHI and EcoRV</p>
+<section id="main" class="container">
+	<div class="row" style="font-size:initial">
+		<div class="12u">
+			<section class="box">
+				<header class="major">
+					<h2>Protocols<br />
+					</h2><hr>
+				</header>
-<p>Agarose gel 1%</p>
+<p id="scroll1">Here we present you all the procedures we did to develop our project. On this page you can find the general protocols. If preferred, you can go directly to the dialy Notebook, the experiments on <i>Nicotiana</i> or the protoplasts experiments by pressing in the buttons above or below (after protocols). We hope you enjoy reading our incredible journey!</p>
+<br/>
+<div>
+				<details id="scrollsect1">
+				    <summary class="button fit">Constructions protocol</summary>
+				    <div class="clsPadding">
+<p><div style="text-align: center;"><img width=600em src="https://static.igem.org/mediawiki/2015/c/c2/Valencia_upv_protocolo_3.png" ></div> </p>
-<p>How to ask and make primers?</p>
+<p><b>2. Ligation in pUPD2:</b></p>
-<ul><li>Select the sequence to amplify and save in FASTA format.</li>
-<li>gbCloning, go to Tools-Domesticator-1º Category</li>
-<li>Add FASTA and select parts.</li>
+<p>The ligations have a total volume of 10 µl. All the parts were mixed together in an eppendorf of 0.2ml. The eppendorf was put in the thermocycler with the programs GB or GG, the differences between them are number of cycles. Explain the cycles!</p>
-<li>On the protocol we have the primers </li>
+<p>*The cells with the asterisk are the ones that are going to be written down and specified in the lab-book. The others cells are constant unless we indicate it specifically on the lab-book.</p>
-<li>The oligos they give us:</li>
-<ul class="ul_2"><li>4 first nucleotides: so the enzyme can recognize without problems</li>
-<li>6 following bingind sites.</li>
-<li>1 extra nucleotide.</li>
-<li>4 overhangs. </li>
-</ul></ul>
-<p>Meeting with Daniel Ramón (Biopolis). </p>
-<p>Ligation with part 2 and 24 of task sheet.</p>
@@ Line 68: / Line 51: @@
 <div class="table-wrapper"><table class="alt">
-<tr><td>PIF6 + PhyB; ?1</td><td>Etr8 CMV_Bxb1_T35S</td></tr>
+<tr><td>DNA; pUPD2</td></tr>
-<tr><td>1µL 892 (PIF &alpha;1)</td><td>1µL 1097 (Etr8 CMV) Pupd2</td></tr>
+<tr><td>1 µl DNA fragment</td></tr>
-<tr><td>1µL 88E (Phy &alpha;2)</td><td>1µL Bxb1 (PuPD)</td></tr>
-<tr><td>1µL ?1 </td><td>1µL Tnos PuPD</td></tr>
-<tr><td>1.2µL Buffer ligase</td><td>1µL &alpha;1</td></tr>
-<tr><td>1µL Bsmb1</td><td>5.8µL H2O</td></tr>
-<tr><td>6.8µL H2O</td><td></td></tr>
-</div></table>
-<p>If we make a digestion of 160 (35S:Renilla:tNOS-35S:P19:tNOS) with EcoRV, we obtain: 2475, 381, 4601 pb.</p>
-<p>If we make a digestion of 896 (Luc:PIF6:PhyB)with EcoRV, we obtain: 11608, 3942 pb.</p>
-</br><h3 style="color:green">June 2015</h3>
-<p>Transform to E.coli from PIF+Phy and Bxb1</p>
-<ul><li>1.5µL of ligation</li>
-<ul class="ul_2"><li>Cuvette on ice</li>
-<li>Competent cells + 1.5µL of ligation</li>
-<li>Pulse (electroporator) at 1500V</li>
-<li>Add 300µL shock medium and put Eppendorf 1h at 37ºC</li>
-</ul></ul>
-<p>Culture on petri dishes the ligations.</p>
-<p>Digest of 160, 289 and the two ligations, PIF+phy and Etr8+BxbI. </p>
-<p>Agarose gel. </p>
-</br><h3 style="color:green">7 June 2015</h3>
-<p>We’ve got white colonies! (from PIF+Phy and Bxb1)</p>
-<p>Pick two colonies from each construction.</p>
-<p>4 tubes</p>
-<ul><li>3.5µL LB each tube</li>
-</ul>
-<p>2)	2 tubes + 3.5µL Kanamycin (K)</p>
-</br><h3 style="color:green">8 June 2015</h3>
-<p>Minipreps of the 4 liquid cultures and digestion to see the band patterns.</p>
-<p>Digestion:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Etr8(CMV):Bxb1:Tnos; ?1</td><td>EcoRI</td><td>6345, 238</td></tr>
-<tr><td>EPIF6 + PhyB-PV16; ?1</td><td>BamHI</td><td>6686, 1439, 2685, 2237</td></tr>
-</div></table>
-<p>Agarose gel was made:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Bxb1 (C1)</td><td>Bxb1 (C2)</td><td>EPIF6 + PhyB-PV16 (C1)</td><td>EPIF6 + PhyB-PV16 (C2)</td><td></td></tr>
-<tr><td>ok</td><td>ok</td><td></td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-</div></table>
-<p>Repeat digestion (errors).</p>
-<p>We don’t have sure the toggle, so we decide to repeat the digestion with other enzyme tomorrow, noticing that the
-colony 2 has better bands pattern.</p>
-<p>Optimized ligation of PIF-Phy-Lac-Renilla-P19</p>
-<ul><li>1 µL vector</li>
-<li>0.8 µL dilution ½ 160</li>
-<li>1.7 µL big part</li>
-<li>1.2 µL BSA</li>
-<li>1.2 µL buffer</li>
-<li>1 µL BsbmI</li>
-<li>1 µL ligase</li>
-<li>4.15 µL H2O</li>
-<li>Ratio 1:2 vector insert</li>
-</ul>
-<p>As Bxb1 was good at the digestion we put 1 µL of LB and 1 µL of Kanamicyne on the tube where it had grown and store at
-ºC to glycerinate later.</p>
-<p>We design primers to binding domain (BD) and PIF.</p>
-<ul><li>Problem: domesticator is introduced in an old pUPD. The new one has different bases. </li>
-<li>Change manually the pUPD bases in the program (Benchling).</li>
-</ul></ul>
-</br><h3 style="color:green">9 June 2015</h3>
-<p>Digestion of the ligation of yesterday containing: EPIF6-PhyB-VP16 (C1 y C2)</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>EPIF6-PhyB-VP16</td><td>PvuII (green buffer)</td><td>3663, 9472pb</td></tr>
-</div></table>
-<p>Agarose gel 1%:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>EPIF6-PhyB-VP16 (C1)</td><td>EPIF6-PhyB-VP16 (C2)</td><td>EPIF6-PhyB-VP16 (C3)</td></tr>
-<tr><td>no</td><td>no</td><td>no</td></tr>
-</div></table>
-<p>We see three bands: 7000, 4000, 1900pb</p>
-<p>Transform optimized ligation (yesterday 8/6)</p>
-<ul><li>3.5 µL ligation product (EPIF6-PhyB-VP16 + Luciferase + Renille + P19)</li>
-<li>40 µL electrocompetent cells.</li>
-<li>Pulse of 1500V</li>
-<li>Store 1h at 37ºC</li>
-<li>Plate culture at agar with Spectinomycin: 50 µL of the transformation.</li>
-</ul>
-</br><h3 style="color:green">10 June 2015</h3>
-<ul><li>Check the primers and order LexA, Gal4, PIF6, LacI, Dronpa.</li>
-<li>Check linker VP16 (88E) and make a primer for it.</li>
-<li>Take out glycerinate of &Omega;2.</li>
-</ul>
-<p>Alfredo’s part is not working.</p>
-<ul><li>Pick colonies of transformation and make liquid culture of E:PIF6:PhyB:VP16:luc:ren (C1-C3).</li>
-</ul>
-<ul><li>Minipreps of liquid culture (PIF + Phy), colonies C3, C4, C5, C6</li>
-<li>Digestion:</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PIF + Phy:VP16</td><td>PvuII (buffer green 10x)</td><td>3663, 9472</td></tr>
-<tr><td>PIF + Phy:VP16</td><td>BamHI</td><td>1939, 2685, 2337, 6674</td></tr>
-</div></table>
-<ul><li>Agarose gel 1% (10 samples, 8 + 2 molecular markers)</li>
-</ul>
-<p>PIF + Phy (PvuII) C3	PIF + Phy (PvuII) C4	PIF + Phy (PvuII) C5	PIF + Phy (PvuII) C6</p>
-<p>no	ok	no	No</p>
-<p>PIF + Phy (BamHI) C3	PIF + Phy (BamHI) C4	PIF + Phy (BamHI) C5	PIF + Phy (BamHI) C6</p>
-<p>no	ok	no	No</p>
-<ul><li>Transformation of <i>Agrobacterium</i> (C58) of the 896 construction (EPIF6-PhyB-VP16 + luciferase). We are not
-going to have the positive control and we won’t be able to quantify (we don’t have Renilla + P19).</li>
-</ul>
-</br><h3 style="color:green">11 June 2015</h3>
-<ul><li>Minipreps of the culture:</li>
-</ul>
-<ul><li>Digestion:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>E:PIF6:PhyB:VP16:luc:ren</td><td>BamHI</td><td>4209, 3756, 6100, 6674</td></tr>
-<tr><td></td><td>EcoRV</td><td>3942, 2989, 2475, 381, 10952</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PIF6:PhyB:VP16:luc:</td></tr>
-<tr><td>ren C1 (BamHI)</td><td>PIF6:PhyB:VP16:luc:</td></tr>
-<tr><td>ren C3 (BamHI)</td><td>PIF6:PhyB:VP16:luc:ren</td></tr>
-<tr><td>C1 (EcoRV)</td><td>PIF6:PhyB:VP16:luc:ren </td></tr>
-<tr><td>C3 (EcoRV)</td></tr>
-<tr><td>??</td><td></td><td></td></tr>
-</div></table>
-<p>Transformation in <i>Agrobacterium</i> of Renilla (160) due to that we could not join this with PIF:phyB and so we will
-do a cotransfection of both plasmids. Make petri dish culture with kanamicyn and rifampicin.</p>
-</br><h3 style="color:green">12 June 2015</h3>
-<p>The petri dish with PIF:phy:luc was taken out the 37ºC room and put into the fridge to pick  colonies tomorrow.</p>
-</br><h3 style="color:green">13 June 2015</h3>
-<ul><li>Pick colonies to make liquid culture:</li>
-<ul class="ul_2"><li>Renilla in agrobacterium: just one colony, it was made liquid culture but check carefully the
-gel.</li>
-<li>It was noticed that the piece 160, renilla, needs a pSub plasmid to replicate itself so we will transform 160 into a
-agrobacterium with this plasmid (C58 pSub).</li>
-</ul><li>Ligation:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>BxbI; alfa1+phyB; alfa2</td></tr>
-<tr><td>1µl BxbI</td></tr>
-<tr><td>1 µl phyB</td></tr>
-<tr><td>1 µl ?2</td></tr>
-<tr><td>4.6 µl H2O</td></tr>
-</div></table>
-<ul><li>Transform renilla (160) into agrobacterium and make </li>
-</ul></ul>
-</br><h3 style="color:green">15 June 2015</h3>
-<ul><li>Repeat the ligation BxbI+35S:E-PIF6:tnos because PIF was ?2</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>BxbI + 35S:E-PIF6:tnos; ?1</td></tr>
-<tr><td>1µl BxbI</td></tr>
-<tr><td>1 µl phyB</td></tr>
-<tr><td>1 µl ?1</td></tr>
-<tr><td>4.6</td><td>µl H2O</td></tr>
-</div></table>
-<ul><li>KDronpa has arrived:</li>
-<ul class="ul_2"><li>Centrifuge it 2-5sec at max velocity.</li>
-<li>Add 50 µl to have a concentration of 20ng/µl</li>
-<li>Mix it with the vortex and spin.</li>
-</ul><li>Ligation: en la libreta pone que se liga a pUPD2</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>KDronpa; pUPD2</td></tr>
-<tr><td>1 µl KDronpa</td></tr>
 <tr><td>1 µl pUPD2</td></tr>
-<tr><td>5.6 µl H2O</td></tr>
+<tr><td>1.2 µl buffer ligase</td></tr>
-</div></table>
+<tr><td>1.2 µl BSA (10x)</td></tr>
+<tr><td>1 µl BsmbI</td></tr>
+<tr><td>1 µl T4 ligase</td></tr>
+<tr><td>5,6 µl H<sub>2</sub>O</td></tr>
-<ul><li>It was not possible to pick colonies of the <i>Agrobacterium</i> transformed because they did not grow. Maybe the
-problem is that with tetraciclyn bacterias grow slowly. Wait 1 day more.</li>
-<li>Transformation of the ligation, BxbI + 35S:E-PIF6:tnos; ?1, into E.coli.</li>
-<li>Make an agar culture in petri dish and let grow 16h at 37ºC.</li>
-</ul>
-</br><h3 style="color:green">16 June 2015</h3>
-<ul><li>Transformation of the ligation, KDronpa, into E.coli.</li>
-<li>Pick colonies of BxbI:E-PIF6 and make liquid culture (C1-C3).</li>
-<li>Primers had arrived, it has been done the resuspension (dilution 1:10)of all of them.</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Primers</td><td>Code </td><td>Template</td><td>Working temperature? ºC</td></tr>
-<tr><td>LacI F</td><td>1</td><td>LacI (858)</td><td>69.7</td></tr>
-<tr><td>LacI R </td><td>2</td><td></td></tr>
-<tr><td>Gal4 F</td><td>3</td><td>We did not take out the glicerynate.</td><td>63.2</td></tr>
-<tr><td>Gal4 </td><td>4</td><td></td></tr>
-<tr><td>LexA F</td><td>5</td><td>LexA (732)</td><td>62.7</td></tr>
-<tr><td>LexA R</td><td>6</td><td></td></tr>
-<tr><td>PIF:VP16 F</td><td>7</td><td>PIF6 (288)</td><td>60.1</td></tr>
-<tr><td>PIFVP16 R</td><td>8</td><td></td></tr>
-<tr><td>NDronpa F1</td><td>9</td><td>Kdronpa</td><td>67.7</td></tr>
-<tr><td>NDronpa R1</td><td>10</td><td></td></tr>
-<tr><td>Dronpa F2</td><td>11</td><td>58.5</td></tr>
-<tr><td>NDronpa R2</td><td>12</td><td></td></tr>
 </div></table>
@@ Line 524: / Line 71: @@
-<ul><li>A PCR with all the primers and the fragments was done, the samples were put in order with the temperature.</li>
+<p><b>8. Ligation in &alpha; or &Omega;:</b></p>
-<ul class="ul_2"><li>The templates were in dilution 1:50, exception of KDronpa that was dilution 1:5 and the primers
-:10.</li>
-</ul></ul>
@@ Line 536: / Line 77: @@
 <div class="table-wrapper"><table class="alt">
-<tr><td>PCR Fusion Taq (50µl)</td></tr>
+<tr><td>DNA1;pUPD2+DNA2;pUPD2 ; &alpha;</td><td>DNA1; &alpha;1+DNA2; &alpha;2; &Omega;</td></tr>
-<tr><td>DNA template (10 µg/µl)</td></tr>
+<tr><td>1 µl DNA1; pUPD2</td><td>1 µl DNA1; &alpha;1</td></tr>
-<tr><td>0.5 µl fusion taq</td></tr>
+<tr><td>1 µl DNA2; pUPD2</td><td>1 µl DNA2; &alpha;2</td></tr>
-<tr><td>2.5 µl primer F</td></tr>
+<tr><td>1 µl &alpha;</td><td>1 µl &Omega;</td></tr>
-<tr><td>2.5 µl primer R</td></tr>
+<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td></tr>
-<tr><td>2 µl NTPs</td></tr>
+<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>31.5 µl H2O</td></tr>
+<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>17 June 2015</td></tr>
-</div></table>
-<ul><li>Pick colonies and make liquid culture of:</li>
-<ul class="ul_2"><li>KDronpa (C1-C4)</li>
-<li>Ligations with the PCR’s products:</li>
-<li>Templates PCR: 1+2, 5+6, 7+8PIF, 7+8VP16, 9+10, 11+12.</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Template PCR; pUPD2</td></tr>
-<tr><td>0.5µl template</td></tr>
-<tr><td>1µl pUPD2</td></tr>
+<tr><td>1 µl BsaI</td><td>1 µl BsmbI</td></tr>
-<tr><td>6.1µl H2O</td></tr>
+<tr><td>4.6 µl H<sub>2</sub>O</td><td>4.6 µl H<sub>2</sub>O</td></tr>
 </div></table>
@@ Line 584: / Line 99: @@
+<p><b>3a. Transformation:</b></p>
+<p>In order to transform the DNA construction the electroporation method was used. </p>
-<ul><li>Minipreps of liquid cultures:</li>
+<p>The method followed is common for E. coli and <i>Agrobacterium</i>. The electroporation cuvette was put in ice 10 minutes before inserting the cells.</p>
-<ul class="ul_2"><li>BxbI:E-PIF6 (C1-C3)</li>
+<p>Frozen cells were taken out of the -80ºC freezer, and they were put immediately into ice. </p>
-</ul><li>Agarose gel with the PCRs:</li>
+<p>1-2 µl of the ligation were taken and added carefully to the electrocompetent cells.</p>
-</ul>
+<p>60 µl of the mix were taken and put into an electroporation cuvette making sure that there were no bubbles. </p>
-<div class="table-wrapper"><table class="alt">
+<p>The cuvette was dried and put in the electroporator, making sure that it did not do a spark. In that case, the process did not work and must be repeated.</p>
-<tr><td>Template</td><td>1+2</td><td>5+6</td><td>7+8PIF</td><td>7+8VP16</td><td>9+10</td><td>11+12</td></tr>
+<p>The voltage is 1500V for E. coli and 1440V for <i>Agrobacterium</i>.</p>
-<tr><td>Band pattern</td><td>1017</td><td>284</td><td>391</td><td>478</td><td>464</td><td>290</td></tr>
+<p>Then with 300 µl of medium the electroporated cells were taken and put into an Eppendorf, letting them grow in the shaker.</p>
-<tr><td>Gel result</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>No DNA</td><td>ok</td></tr>
+<p>SOC medium was used for E.Coli and they were put at 37ºC for 1h.</p>
-</div></table>
+<p>LB medium was used for <i>Agrobacterium</i> and they were grown for 2h at 27ºC.</p>
-<ul><li>Transformation in E.coli of the correct ligations:</li>
+<p><b>3b. Petri dish culture:</b></p>
-<ul class="ul_2"><li>1+2, 5+6, 7+8PIF, 7+8VP16, 11+12</li>
+<p>Depending on the plasmid with which the bacteria was transfected, agar dishes with the specific antibiotic were needed to make the petri dishes cultures.   </p>
-<li>Put in cloranfenicol petri dishes. </li>
+<ul><li><i>E. coli</i>-pUPD2 plasmids: chloramphenicol.</li>
-</ul></ul>
+<li><i>E. coli</i>-Alpha 1 and 2: kanamycin.</li>
-</br><h3 style="color:green">18 June 2015</h3>
+<li><i>E. coli</i>-Omega 1 and 2: streptomycin</li>
-<ul><li>Minipreps of the liquid cultrures:</li>
+<li><i>Agrobacterium</i>: rifampicin + the specific one for each construction.</li>
-<ul class="ul_2"><li>KDronpa (C1-C4)	</li>
-</ul><li>Digestions:</li>
 </ul>
-<p>KDronpa	EcoRI	2800</p>
+<p>The procedure was made in the laminar flux cabinet. The spread plate method is done with 50-40 µl of the bacteria culture that is in the eppendorf. It was spread with the glass dipstick. After that the plates were put for 16h approximately in 37ºC for E. coli and 32h at 28ºC for <i>Agrobacterium</i>. </p>
-<ul><li>Gel:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Kdronpa C1</td><td>Kdronpa C2</td><td>Kdronpa C3</td><td>KdronpaC4</td></tr>
-<tr><td>no</td><td>no</td><td>ok</td><td>no</td></tr>
-<tr><td>Etr8:BxbI:phyB C1</td><td>Etr8:BxbI:phyB C2</td><td>Etr8:BxbI:phyB C3</td><td></td></tr>
-<tr><td>No</td><td>no</td><td>no</td><td></td></tr>
-</div></table>
-<p>We discovered that the construction with BxbI did not go well because our lab college gives us the wrong piece. </p>
-<ul><li>Take glicerynates out:</li>
-<ul class="ul_2"><li>Gal4; pUPD (731)</li>
-<li>?2</li>
-<li>PromotersinATG (GB00552)</li>
-<li>Renilla (160)(159)(109)</li>
+<p><b>4. Liquid culture:</b></p>
-</ul><li>PCR:</li>
+<ul><li>For <i>Escherichia coli</i>:</li>
 </ul>
-<div class="table-wrapper"><table class="alt">
+<p>The mix was grown 16h at 37ºC in the shaker.</p>
-<tr><td>NDronpa</td></tr>
+<ul><li>For <i><i>Agrobacterium</i> tumefaciens</i>:</li>
-<tr><td>2.5 µl (9+10) primer F</td></tr>
-<tr><td>2.5 µl (11+12) primer R</td></tr>
-<tr><td>2 µl NTPs</td></tr>
-<tr><td>0.2 µl Taq</td></tr>
-<tr><td>10 µl Buffer</td></tr>
-<tr><td>31.5</td><td>µl H2O</td></tr>
-</div></table>
-<ul><li>Ligations:</li>
 </ul>
-<div class="table-wrapper"><table class="alt">
+<p>The mix was grown 32h at 28ºC in the shaker.</p>
-<tr><td>Etr8:BxbI:T35S; &alpha;1</td><td>Template PCR; pUPD2</td></tr>
-<tr><td>1 µlEtr8</td><td>0.5µl template</td></tr>
-<tr><td>1 µl BxbI</td><td>1µl pUPD2</td></tr>
+<p><b>5. Minipreps:</b></p>
-<tr><td>1 µl T35S</td><td>6.1µl H2O</td></tr>
-<tr><td>5.8 µl H2O</td><td></td></tr>
-<tr><td></</td></tr>
+<p>In order to do the minipreps -extraction of the plasmids out of <i>E. coli</i> the protocol of the Omega kit (Plasmid DNA Mini Kit I Spin Protocol) was used. The steps to do it are:</p>
-<tr><td></td></tr>
+<p>1.	Centrifuge at 10.000xg for 1minute at room temperature the liquid medium with the growed bacteria.</p>
-<div class="table-wrapper"><table class="alt">
+<p>2.	Decant or aspirate and discard the culture media.</p>
-<tr><td>Templates PCR: 1+2, 5+6, 7+8PIF, 7+8VP16</td></tr>
+<p>3.	Add 250 µl SolutionI/RNase A. Vortex or pipet up and down to mix thoroughly. Complete resuspension of cell pellet is vital for obtaining goo yields.</p>
-</br><h3 style="color:green">19 June 2015</h3>
+<p>4.	Tranfer suspension into a new 1.5mL microcentrifuge tube.</p>
-<ul><li>We do a PCR with the normal Taq polymerase.</li>
+<p>5.	Add 250 µl Solutions II. Invert and gently rotate the tube several times to obtain a clear lysiate. A 2-3 minute incubation may be necessary.</p>
-<ul class="ul_2"><li>1µl of DNA’s template (9+10, 9+12 and 11+12)</li>
+<p>6.	Add 350 µl Solution III. Inmediately invert several times until a flocculent white precipitate forms.</p>
-<li>2µl of specific buffer</li>
+<p>7.	Centrifuge at maximum speed (>13.000xg) for 10 minutes. Acompact white pellet will form. Promptly preceed to the next step.</p>
-<li>2µl of NTPs</li>
+<p>8.	Insert a HiBind DNA Mini Column into a 2 mL Collection tube.</p>
-<li>1µl primer forward</li>
+<p>9.	Transfer the cleared supernatant from Step 8 CAREFULLY aspirating it into the HiBind DNA Mini Column. Be careful not to disturb the pellet and that mo cellular debris is transferred the the HiBind DNA Mini Column.</p>
-<li>1µl primer reverse</li>
+<p>10.	Centrifuge at maximum speed for 1 minute.</p>
-<li>0.5 µl of Taq</li>
+<p>11.	Discard the filtrate and reuse the collection tube.</p>
-<li>12.5 µl H2O</li>
+<p>12.	Add 500 µl HBC Buffer.</p>
-<li>These quantities multiplied by 3.</li>
+<p>13.	Centrifuge at maximum speed for 1 minute.</p>
-</ul><li>Minipreps of the yesterday’s glycerinated cultures.</li>
+<p>14.	Discard the filtrate and reuse collection tube.</p>
-<li>To do the digestions we add in each eppendorf.</li>
+<p>15.	Add 700 µl DNA Wash Buffer .</p>
-</ul>
+<p>16.	Centrifuge at maximum speed for 1 minute.</p>
-<div class="table-wrapper"><table class="alt">
+<p>17.	Discard the filtrate and reuse the collection tube.</p>
-<tr><td>Minipreps:</td><td>Enzime</td><td>Band pattern</td></tr>
+<p>18.	Centrifuge the empty HiBind DNA Mini Column for 2 minutes at maximum speed to dry the column.</p>
-<tr><td>159 pDGB1_?2 renilla</td><td>EcoRV</td><td>2909, 2475,882, 812, 381</td></tr>
+<p>19.	Transfer the HiBind DNA Mini Column to a clean 1.5 mL microcentrifuge tube.</p>
-<tr><td>Entry vector, ?2</td><td>EcoRV</td><td>6652, 621</td></tr>
+<p>20.	Add 30-100 µl Elution Buffer or sterile deionized water directly to the center of the column membrane.</p>
-<tr><td>552 pP35s NoATG, pUPD</td><td>EcoRI</td><td>2997, 1090</td></tr>
+<p>21.	Let sit at room temperature for 1 minute.</p>
-<tr><td>160 renilla pDGB1, a2 </td><td>EcoRV</td><td>4601, 2475, 381</td></tr>
+<p>22.	Centrifuge at maximum speed fot 1 minute.</p>
-<tr><td>731 pUPD pGal4BD (CDS)</td><td>EcoRI</td><td>2997, 2493</td></tr>
-<tr><td>109</td><td>GB1_a1 355:renilla:Tnos</td><td>EcoRI</td><td>2580, 2493</td></tr>
-</div></table>
+<p><b>6a. Digestion:</b></p>
+<p>After doing the miniprep the DNA was obtained. The next components were mixed up in a 200 µl eppendorf. After the mix was done it stayed at 37ºC, 1h.</p>
-<ul><li>We make an agarose gel with the digestions made before and the PCR of KDronpa. </li>
-</ul>
 <div class="table-wrapper"><table class="alt">
-<tr><td>159</td><td>160</td><td>?2</td><td>552</td><td>731</td><td>109</td><td>9+10</td><td>9+12</td><td>11+12</td></tr>
+<tr><td>1 µl of the DNA</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>no</td><td>ok</td><td>ok</td></tr>
+<tr><td>1 µl specific buffer</td></tr>
-</div></table>
+<tr><td>0.5 µl of the specific enzyme</td></tr>
+<tr><td>7.5 µl of H<sub>2</sub>O</td></tr>
-<ul><li>Transformation of the ligations:</li>
-<ul class="ul_2"><li>50 µl of electrocompetent cell</li>
-<li>1.5 µl of ligation</li>
-<li>Put 1 min before the cubettes in ice </li>
-<li>Make the transformation (1500V)</li>
-<li>Put the transformed cells 1h at 37ºC</li>
-</ul></ul>
-<ul><li>We made an stack of Cloranfenicol petri dishes</li>
-<ul class="ul_2"><li>250ml  LB aga</li>
-<li>X-gal (1:500): 500 µl</li>
-<li>Iptg (1:1000): 250 µl</li>
-<li>Cloranfenicol (1:2000): 125 µl</li>
-</ul></ul>
-</br><h3 style="color:green">20 june 2015</h3>
-<p>We have White colonies of renilla! Also of Etr8 + Bxb1</p>
-<p>We have also pUPD colonies but they are so close to the blue ones that we can’t pick anyone.So we make strakes in
-another plates to have the colonies separated.</p>
-<ul><li>We make a liquid culture of Agro of Renilla.</li>
-<ul class="ul_2"><li>5ml of LB agar</li>
-<li>5 µl rifampicine</li>
-<li>5 µl of kanamicine</li>
-<li>5 µl tetracycline</li>
-<li>Incubate for 2 days (48h) at 28ºC.</li>
-</ul></ul>
-</br><h3 style="color:green">21 June 2015</h3>
-<ul><li>Pick colonies of and put into a liquid medium of 3 ml of LB agar, 3 µl of each antibiotic (kanamicine,
-spectomicine, cloranfenicol):</li>
-<ul class="ul_2"><li>Plates (17/06/15): PIF (C1, C2) (with cloranfenicol), VP16 (C1, C3) (with cloranfenicol), LacI (C1,
-C2, C3) (with cloranfenicol)</li>
-<li>Plates (19/06/15): Bxb1 (C1, C2, C3) (with kanamicine), VP16 (C4, C5) (with cloranfenicol), LacI (C1, C2) (with C1,
-C2) (with cloranfenicol), PIF (C1, C2, C3, C4, C5) (with cloranfenicol), LexA (C1, C2) (with cloranfenicol).</li>
-</ul><li>We take out two glicerynates of GFP and BFP (of the Alfredo’s box)</li>
-</ul>
-</br><h3 style="color:green">22 June 2015</h3>
-<ul><li>We made minipreps of the liquid culture of the day before:</li>
-<ul class="ul_2"><li>LacIBD, pUPD (C1-C5)</li>
-<li>LexABD, pUPD (C1, C2)</li>
-<li>Etr8(CMV):Bxb1 (C1-C3)</li>
-<li>PIF6,pUPD (C1-C5)</li>
-<li>VP16, pUPD (C1, C4, C5)</li>
-</ul></ul>
-<ul><li>Make the digestions of all the minipreps:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD, pUPD</td><td>NotI</td><td>2046, 1053</td></tr>
-<tr><td>LexABD, pUPD </td><td>NotI</td><td>2046, 321</td></tr>
-<tr><td>Etr8(CMV):Bxb1 </td><td>NotI</td><td>1532, 1290, 5896</td></tr>
-<tr><td>PIF6,pUPD </td><td>NotI</td><td>2046, 407</td></tr>
-<tr><td>VP16, pUPD </td><td>NotI</td><td>2046, 500</td></tr>
 </div></table>
@@ Line 874: / Line 229: @@
-<ul><li>Viral system:……….</li>
+<p>1 µl of loading buffer is needed for each 5 µl of the digestion mix, so they were added 2 µl of loadding buffer (6x).</p>
-<li>We received the reported Bxb1!</li>
-<ul class="ul_2"><li>500ng of sample</li>
-<li>Centrifuge at 3000rpm for 5 seconds (spin).</li>
-<li>Add 50 µl H2O</li>
-<li>Shake it and let at 50ºC for 20min</li>
-<li>Make a PCR of Gal4 and NDrompa (9-10), the primers of NDrompa are aliquoted</li>
-</ul><li>…..</li>
-</ul>
-<p>Make the gel with all the digestions writed before.</p>
+<p>These are the specific enzymes and buffers for each type of plasmid.</p>
@@ Line 900: / Line 237: @@
 <div class="table-wrapper"><table class="alt">
-<tr><td>Lac1</td><td>Lac2</td><td>Lac3</td><td>Lac4</td><td>Lac5</td><td>Lex1</td><td>Lex2</td><td>Bxb1,1</td><td>Bxb2,
+<tr><td>Plasmid</td><td>Enzyme</td><td>Buffer</td></tr>
-</td><td>Bxb1,3</td></tr>
+<tr><td>pUPD2</td><td>Not I</td><td>Orange</td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>no</td><td>no</td><td>ok</td><td>ok</td><td>no</td></tr>
+<tr><td>Alpha  </td><td>EcoRI</td><td>Specific </td></tr>
-<tr><td>PIF1</td><td>PIF2</td><td>PIF3</td><td>PIF4</td><td>PIF5</td><td>VP16,1</td><td>VP16,4</td><td>VP16,5</td><td></td
+<tr><td>Omega </td><td>BamHI</td><td>Specific </td></tr>
-></tr>
-<tr><td>No</td><td>no</td><td>-</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td></td></tr>
-<tr><td>PCRS</td><td>…</td><td>…</td><td>…</td><td></td><td></td><td></td></tr>
 </div></table>
-<p>					</p>
-<ul><li>We make ligations of:</li>
-<ul class="ul_2"><li>Etr8(CMV):BxbI in a1 + PhyB:P16 in a2, ?1</li>
+<p>The plasmids can also be cut with other enzymes if it is necessary to check the construction.</p>
-<li>LacIBD in pUPD2 + PIFBDless+promoter+terminator, a1</li>
-<li>KDrompa in pUPD2 + LacBD+promoter+terminator, a1</li>
-<li>Gal4BD, pUPD2</li>
+<p><b>6b. Gel:</b></p>
-<li>Reporter of BxbI, pUPD2</li>
-</ul></ul>
-<ul><li>Tomorrow we have to take out pUPD of constitutive promoters, terminators and GFP (CDS).</li>
+<p>The gel was made with buffer + dilution 1:1000 of ethidium bromide and a proportion of 0.1% of agarose.</p>
-</ul>
+<p>The small gels had 40ml of buffer + 0.4 µl of ethidium bromide and 0.4g of agarose.</p>
-</br><h3 style="color:green">23 June 2015</h3>
+<p>After waiting 1h to let the gel cool down, the ladders of 100bp and 1kbp are put one on each side of the gel, and the digestions in between the ladders. </p>
+<p>The voltage to apply is 120V.</p>
+<p>It was written in a table the DNA fragments obtained and the words “ok “ or “no” depending on if the results are correct or not. Example:</p>
-<ul><li>Transformations in E.Coli of the 5 ligations done yesterday and two more transformations of 5+6(1) and 5+6(2)
-which are the ligations in pUPD of the 18/06. </li>
-<li>We put 50 µl of the transformations in the plates. Put in 37ºC.</li>
-<ul class="ul_2"><li>Etr8(CMV):Bxb1 in a1 + PhyB:P16 in a2, ?1</li>
-<li>LacIBD in pUPD2 + PIFBDless+promoter+terminator, a1</li>
-<li>KDrompa in pUPD2 + LacBD+promoter+terminator, a1</li>
-<li>Gal4BD, pUPD2</li>
-<li>Reporter of Bxb2, pUPD</li>
-<li>LexABD (5+6(1)), pUPD</li>
-</ul></ul>
-<ul><li>We have taken out of the -80ºC fridge the glycerinate of GFP, pUPD/ampicilina/GB0059.</li>
-<li>The liquid culture of Renilla (rifampicina/kanamicia/tetraciclina) doesn’t grow before the two days required. So we
-decide to put two new colonies in une tube with the three antibiotics and another with rifampicina and kanamicine. Asun
-say that the tetracycline slow down the growth of Agro.</li>
-<li>The 4 liquid cultures of LexA+IPTG/+gal are all blue: throw them.</li>
-<li>We ordered again the primer nº10 (NDronpa R1). Changing one codon in 3’ and delete another in 5’.</li>
-</ul>
-</br><h3 style="color:green">24 June 2015</h3>
-<p>Pick colonies of the plates done yesterday and pass them into a liquid media: 3 µl of LB, 3 µl of antibiotics (K,
-Spect, Clor).</p>
-<ul><li>LacIBD+PIF, a1 (C1, C2)</li>
-<li>Gal4BD, pUPD2 (C1)</li>
-<li>RepBxb1, pUPD2 (C1, C2, C3)</li>
-<li>LacIBD+KDonpa, a1 (C1, C2)</li>
-<li>Etr8(CMV)+Bxb1+phyB+VP16, ?1 (C1)</li>
-<li>LexABD1, pUPD (C1-C4)</li>
-<li>LexABD2, pUPD. No colonies.</li>
-</ul></ul>
-<p>The viral systems cultures of Agro for the color mosaics are ready before 2 days at 28ºC. We can make the
-Agroinfiltration.</p>
-<p>Buffers of Agroinfiltration:</p>
-<ul><li>First we have to prepare and ajust the pH of the buffer MES and the buffer MgCl.</li>
-<li>MES (10x), 100nM; ph=5,6 (adding NaOH). Make 1L.</li>
-<li>MgCl (100x), 1M. Make 100ml.</li>
-<li>Solution to agroinfiltration: 10ml of MES(10x) + 1ml of MgCl (100x) + 100 µl of DMSO+acetosiningona and finally
-“enrasar” to 100ml.</li>
-<li> 19.6mg of acetosiningona for 500 µl of DMSO</li>
-</ul></ul>
-<ul><li>Ligation:</li>
-</ul>
 <div class="table-wrapper"><table class="alt">
-<tr><td>ETR8(CMV):Bxb1(a1)+phyB+VP16(a2); ?1 </td><td>Gal4BD(pcr) + pUPD2</td></tr>
+<tr><td>DNA1</td><td>DNA2 C1</td><td>DNA2 C2</td><td>DNA4</td></tr>
-<tr><td>1.5 µl etr8:Bxb1</td><td>1 µl Gal4 PCR</td></tr>
+<tr><td>ok</td><td>no</td><td>no</td><td>ok</td></tr>
-<tr><td>1.5 µl 88E (phyB+VP16)</td><td>1 µl pUPD2</td></tr>
-<tr><td>1 µl ?1</td><td>1.2 buffer T4 ligase</td></tr>
-<tr><td>1.2 µl buffer T4 ligase</td><td>1 µl ligase</td></tr>
-<tr><td>1 µl ligase</td><td>1.2 µl BSA</td></tr>
-<tr><td>1.2 µl BSA</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl BsmbI</td><td>5,6 µl H2O</td></tr>
-<tr><td>3.6</td><td>µl H2O</td><td></td></tr>
 </div></table>
@@ Line 1,044: / Line 279: @@
-<p>Quantification of DNA:</p>
+<p><b>7. Sequence:</b></p>
-<ul><li>pUPD GFF (0059): 249 ng/µl</li>
-<li>?2: 238 ng/µl</li>
-<li>Alfredo’s pUPD2, domesticator: 102 ng/µl</li>
-<li> iGEM704: 405 ng/µl</li>
-<li>IGEM735: 403 ng/µl</li>
-<li>552 AMP 35S noATG: 45 ng/µl</li>
-<li>PIF (C5), pUPD2: 119 ng/µl</li>
-<li>pD6B3, ?2 (22/06): 158 ng/µl</li>
-<li>LacIBD (C1), pUPD (22/06): 129 ng/µl</li>
-<li>109k renillaDC: 49 ng/µl</li>
+<p>To check if the plasmid obtained has the proper construction, a Sanger sequencing was made. </p>
-<li>IGEM 534: 13.6 ng/µl</li>
+<p>The IMBCP has its own sequencing service.</p></p><br/>
+				    </div>
+				</details>
+				<details>
+				    <summary class="button fit">Agroinfiltration protocol</summary>
+				    <div class="clsPadding">
+				    	<p><p>The agroinfiltration is a process that consist of introducing <i><i>Agrobacterium</i> tumefaciens</i> into a leaf plant by is underside. <i><i>Agrobacterium</i> tumefaciens</i> is a bacteria that causes the formation of tumours in some plant species like <i>Nicotiana benthamiana</i>, the one that we are working on. This bacteria carried the plasmid that have the DNA construction we want to test and as it infects the cell plants produce a transitory expression of our DNA piece. </p>
-<li>VP16 (C1), pUPD2:102 ng/µl</li>
+<p>So to start the process of the agroinfiltration first of all we have to grow <i>Agrobacterium</i> in liquid culture two days, then refresh two times this first culture taking 5µl of the previous culture. The refresh cultures are only one day incubating at 28ºC. After this starts the procedure:</p>
-<li>IGEM 1097: 409 ng/µl</li>
+<p>1.	Centrifuge the <i>Agrobacterium</i>cultures 10min at 3000rpm.</p>
-<li>K-donpa (C3), pUPD2 (18/06): 174 ng/µl</li>
+<p>2.	While doing this prepare the agroinfiltration solution. It is made of 10ml of MES 10x (100mM, pH 5.6) + 1ml MgCl2 (1M) + 100µl of acetosyringone solution (200mM) it is composed by 9.8mg of acetosyringone dilute with 250µl of DMSO. Add water up to 100ml. </p>
-<li>IGEM 858: 487 ng/µl</li>
+<p>3.	Eliminate the supernatant of the cultures and then add 5ml of the agroinfiltration solution. Resuspend the bacteria and let them grow in dark in the shaker. </p>
-<li>731AMP Gal4 (19/06): 81 ng/µl</li>
+<p>4.	Measure the OD (optical density). To do this the <i>Agrobacterium</i>culture is diluted in proportion 1:10 so it is put 900 µl of agroinfiltration solution and 100 µl of bacteria culture and then measure in the spectofotometer. Depending on the OD obtained the culture will be diluted with a quantity that gets the ODs to 0.2 (when infiltrating viral system the OD has to be 0.1).</p>
-<li>IGEM pUPD2 domesticator: 87 ng/µl</li>
+<p>5.	The dilute bacteria is put in eppendorfs and are ready to agroinfiltrate.</p>
-<li>PIF+phy8 (c1) (08/06): 108 ng/µl</li>
+<p>Tips to agroinfiltrate:</p>
-<li>160 renilla, a2 (19/06): 46 ng/µl</li>
+<ul><li>Do the infiltration on the young leafs without rough surface. </li>
-<li>159 renilla, ?2 (19/06): 149 ng/µl</li>
+<li>Put the syringe with the solution that has bacteria in the undarside and gently introduce the liquid making also a bit of presure with the finger in the adaxial surface of the leaf.</li>
-<li>Etr8:Bxb1 (C1)(22/06): 149 ng/µl</li>
+<li>Change the gloves and the syringe each time you change construction that wants to be agroinfiltrated.</li>
-<li>IGEM 732: 422 ng/µl</li>
+<li>Take the plants out in baches to avoid that due to de hot ambient they close their pores. </li>
 </ul></ul>
-<p>Measurement of the OD:</p>
-<ul><li>first we have to </li>
-</ul></ul>
+<p> </p>
+				    	</p><br/>
+				    </div>
+				</details>
+				<details>
+				    <summary class="button fit">Luciferase assay protocol</summary>
+				    <div class="clsPadding">
+				    	<p><p>Before  start:</p>
-</br><h3 style="color:green">25 June 2015</h3>
+<p>This procedure is done with the Promega; kit (Dual-Luciferase Reporter Assay System).</p>
-<p>Minipreps of the liquid culture:</p>
+<p>First of all is needed to agroinfiltrate the plant and let them for 2 o three days depending on how the experiment is raised. Normally in this days the plants are in darkness because our pieces to tests activates with different wavelegth of ligths. After two days discs are made, trying to take the maximum agroinfiltrated area without any nerve. The discs are put in the specific plate depending on in which ligth condition they need. The samples are taken during one or two days after the discs were made and inmediately the are put in liquid nitrogen and the storage in the -80ºC fridge.</p>
-<ul><li>We don’t observed growth in LacIBD+PIF and LaciBD+K-donpa.</li>
+<p>The steps to follow are:</p>
-</ul></ul>
+<p>1.	The Passive lysis buffer 1x is prepared. It is used 200µl per disc of leaf. The passive lysis buffer is 5x so diluted them with destilled water, always manipulate in ice.</p>
-<p>Digestion of the minipreps and do the gel:</p>
+<p>2.	Grind the freeze sample with a machine that shake the eppendorfs that had to have previusly two little metal balls or with plastic maces. </p>
+<p>3.	Add to the eppendorf 150µl of passive lysis buffer 1x.</p>
+<p>4.	Mix it with the vortex avoiding that they melt. Do this step in cold the maximum time possible.</p>
-<div class="table-wrapper"><table class="alt">
+<p>5.	The samples are centrifuged in cold during 15min at 13200rpm.</p>
-<tr><td>Gal4BD, pUPD2</td><td>NotI</td><td>2046, 282</td></tr>
+<p>6.	A dilution 2:3 is made with the extract, to do that put in a new eppendorf 36µl of passive lyssis buffer 1x and 24µl of sample.</p>
-<tr><td>RepBxb1, pUPD2</td><td>NotI</td><td>2046, 460</td></tr>
+<p>7.	The opaque plate to use in the luminometer is taken. 40 µl of Luciferase is added in each well.</p>
-<tr><td>Etr8(CMV):Bxb1 + phyB,a1</td><td>BamHI</td><td>6674, 2237, 2806, 1174</td></tr>
+<p>8.	10 µl of sample is added too. Wait 10min. During this time turn and configurate the luminometer.</p>
-<tr><td>LexABD, pUPD2</td><td>NotI</td><td>2046, 321</td></tr>
+<p>9.	The luciferase activity is mesured.</p>
-<tr><td>9+10, pUPD2</td><td>NotI</td><td>464</td></tr>
+<p>10.	40 µl/sample +1extra of Dual Glo (1x) was prepared . The sustrate is at 50x and it is at –20ºC, the buffer to dilute it is in the fridge.</p>
-</div></table>
+<p>11.	After the first masure is done add to the wells 40 µl of Dual Glo, let it 10 min and measure the Renilla.</p>
+<p>12.	Take the data obtained and analyze it. </p>
-<p>Gel:</p>
+<p>Things to keep in mind for the next experiment:</p>
+<ul><li>The luminimeter (machine to measure the luminescence) has to be ready before start adding the reactants to the samples because it needs 10min to be ready.</li>
-<div class="table-wrapper"><table class="alt">
+<li>Set the timer (10min) with the first sample of luciferase and add the reactant to the other samples as quick as possible. </li>
-<tr><td>Etr8:Bxb1</td><td>Lex1</td><td>Lex2</td><td>Lex3</td><td>Lex4</td><td>Rep1</td><td>Rep2</td><td>Rep3</td><td>Gal4
-C1</td><td>PCR 9+10</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>no</td><td>no</td><td>ok</td><td>ok</td><td>ok</td><td>no</td><td>ok</td></tr>
-</div></table>
-<ul><li>We make a PCR of the Fusion Taq pH (proof-reading) to prove that the primer received number 10. This new one
-works! Amplify the sequence of N-donpa (R1).</li>
-<li>Refresh the cultures of Agro (28ºC). We pick 7.5 µl of the previous culture. And put into a new liquid media with
-Rifampicine and Kanamicine for 2 days and 28ºC.</li>
-<li>Ligations:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>N-dronpa</td><td>Rep GFP</td><td>Gal4</td><td>LexA</td></tr>
-<tr><td>1 µl PCR 9+10</td><td>1 µl Rep Bxb1</td><td>1 µl PCR 3+4</td><td>1 µl PCR 5+6</td></tr>
-<tr><td>1 µl PCR11+12</td><td>1 µl promoter without ATG</td><td>1 µl pUPD2</td><td>1 µl pUPD2</td></tr>
-<tr><td>1 µl pUPD2</td><td>1 µl Tnos</td><td></td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td><td>1.2 µl buffer
-ligase</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsaI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>4,6 µl H2O</td><td>3,6 µl H2O</td><td>5,6 µl H2O</td><td>5,6 µl H2O</td></tr>
-<tr><td></td><td>1 µl a2</td><td></td></tr>
-<tr><td>Etr8:Bxb1+phyB</td><td></td></tr>
-<tr><td>1 µl Etr8:Bxb1</td><td></td></tr>
-<tr><td>1 µl 88E</td><td></td></tr>
-<tr><td>1µl ?1</td><td></td></tr>
-<tr><td>1.2 µl buffer ligase</td><td></td></tr>
-<tr><td>1.2 µl BSA</td><td></td></tr>
-<tr><td>1 µl BsmbI</td><td></td></tr>
-<tr><td>1 µl T4 ligase</td><td></td></tr>
-<tr><td>3,6 µl H2O</td><td></td></tr>
-</div></table>
-<p>We transform the ligations in E.Coli ant pass them into agar plates with cloranfenicol for all of them except the
-ligation of Etr8:Bxb1+phy that goes with bhnfnfg</p>
-</br><h3 style="color:green">26 June 2015</h3>
-<p>We do again the two ligations that didn’t gone?</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Rep GFP</td><td>LacI BD+PIF6</td></tr>
-<tr><td>1 µl Rep Bxb1</td><td>1 µl LACIBD, pUPD</td></tr>
-<tr><td>1 µl promoter without ATG</td><td>1 µl PIF6, pUPD</td></tr>
-<tr><td>1 µl Tnos</td><td>1 µl promoter</td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1 µl T35</td></tr>
-<tr><td>1.2 µl BSA</td><td>1 µl a1</td></tr>
-<tr><td>1 µl BsaI</td><td>1.2 µl buffer BsaI</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1.2 µlBSA</td></tr>
-<tr><td>2.6 µl H2O</td><td>1 µl BsaI</td></tr>
-<tr><td>1 µl a2</td><td>1 µl ligase</td></tr>
-<tr><td>1µl GFP (0059)</td><td>2.6 µl H2O</td></tr>
-</div></table>
-<p>We make a gel of LAcI+PIF6 (C1 and C2). Both of them present the fragment of the vector at 6000 pb but none of them at
-bp which is the insert one.</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD+PIF; a1</td><td>EcoRI</td><td>6345, 1997, 641</td></tr>
-</div></table>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD+PIF C1</td><td>LacIBD+PIF C2</td></tr>
-<tr><td>no</td><td>no</td></tr>
-</div></table>
-<p>Measurement of the ODs of phyB+PIF+luc and renilla+P19.</p>
-<ul><li>phyB+PIF+luc: o.35 (1:2)</li>
-<li>Ren+P19: 0.34 (1:2)</li>
-<li>Final volume= 2</li>
-<li>CCo= 0.35*2</li>
-<li>CCf= 0.2</li>
-<li>Ecuation=> Vo*CCo=Vf*CCf</li>
-<li>So we obtain that Vo(LacI+PIF6)=1.429 µl and Vo(ren)= 1.412 µl.</li>
 </ul></ul>
-<ul><li>Ligation of: </li>
+<p> </p>
+				    	</p><br/>
+				    </div>
+				</details>
+				<details>
+				    <summary class="button fit">Western blot protocol</summary>
+				    <div class="clsPadding">
+<p><b><u>DAY 1</u></b></p>
-</ul>
+<p><b>PROTEIN EXTRACTION</b></p>
-<div class="table-wrapper"><table class="alt">
+<p>1.	Harvest agroinfiltrated leaves. Grind the harvested material in liquid N2. You can store ground tissue at -80ºC.</p>
-<tr><td>LacIBD,pUPD + K-donpa, pUPD</td></tr>
+<p>2.	Weigh around 100 mg of ground tissue in a 1.5 ml tube. Keep sample frozen!</p>
-<tr><td>1 µl 35S</td></tr>
+<p>3.	Add 3 vol. ice-cold extraction buffer to each sample (300 µl buffer/100 mg tissue).</p>
-<tr><td>1 µl LacIBD,pUPD2</td></tr>
+<p>4.	Mix thoroughly by vortexing for a few seconds. Transfer samples to ice. Repeat vortexing a few times (cooling the sample in between) till sample is completely thaw.</p>
-<tr><td>1 µl K-dronpa, pUPD</td></tr>
+<p>5.	Centrifuge the extract for 15’, at > 12000xg, 4ºC.</p>
-<tr><td>1 µl T35S</td></tr>
+<p>6.	Transfer the supernatant to a fresh 1.5 ml tube. Samples should be kept cold at all times, work on ice!</p>
-<tr><td>1 µl a1</td></tr>
-<tr><td>1.2 µl buffer T4 ligase</td></tr>
-<tr><td>1 µl BsaI</td></tr>
+<p><b>SDS-PAGE</b></p>
-<tr><td>1 µl T4 ligase</td></tr>
-<tr><td>2.6 µl H2O</td></tr>
-</div></table>
-<ul><li>We make the agorinfiltration of (…..) to start checking if the plant react to the different ..</li>
-</ul>
-</br><h3 style="color:green">27 June 2015</h3>
-<p>Transformation in E.coli of LacIBD+K-Dronpa, a1</p>
-<p>We Put into plates LexABD and Etr8(CMV):Bxb1:GFP again and also LAcIBD+K-Dronpa.</p>
-<p>We make liquid culture of:</p>
-<ul><li>RepBxb1:GFP (C1-C4)</li>
-<li>LacIBD+PIF (C1-C5)</li>
-<li>N-Dronpa (C1-C4)</li>
-<li>Gal4BD (C1-C5)</li>
-<li>LexA</li>
-</ul></ul>
-</br><h3 style="color:green">28 June 2015</h3>
-<p>We do the minipreps of the liquid cultures that have grown.</p>
-<ul><li>RepBxb1:GFP (C1 and C2)</li>
-<li>LacIBD+PIF (C1-C4)</li>
-<li>N-Dronpa (C1-C4)</li>
-<li>Gal4BD (C1-C5)</li>
-<li>LexA: didn’t grow</li>
-</ul></ul>
-<p>Do the digestions of the minipreps:</p>
+<p>1.	Sample Mix Preparation ( for 10 µl final volume, scale up as necessary):</p>
@@ Line 1,368: / Line 401: @@
 <div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD+PIF, a1</td><td>EcoRI</td><td>6345, 1997, 641</td></tr>
+<tr><td>Protein extract</td><td>1 to 6.5 µl</td></tr>
-<tr><td>RepBxb1:GFP, ?2</td><td>HindIII</td><td>6345, 2683</td></tr>
+<tr><td>NuPAGE LDS Sample buffer (x4)</td><td>2.5 µl</td></tr>
-<tr><td>Gal4BD; pUPD2</td><td>NotI</td><td>2681, 644</td></tr>
+<tr><td>NuPAGE LDS reducing agent (x10)</td><td>1 µl (use only for reducing conditions)</td></tr>
-<tr><td>N-Dronpa; pUPD2</td><td>NotI</td><td>2046, 744</td></tr>
+<tr><td>Ultrapure H<sub>2</sub>O</td><td>0 to 5.5 µl</td></tr>
 </div></table>
@@ Line 1,380: / Line 413: @@
+<p>Mix by vortexing. Heat at 72ºC<sup>(*)</sup> for 10’. Spin briefly to collect everything at the bottom of the tube. Keep samples on ice.</p>
+<p>2.	Assembling the gel and loading the samples:</p>
-<p>Make the gel.</p>
+<ul><li>Prepare 800 ml MES SDS 1x running buffer</li>
-<div class="table-wrapper"><table class="alt">
-<tr><td>RepBxb1:GFP C1</td><td>RepBxb1:GFP C2</td><td>LacIBD+PIF C1</td><td>LacIBD+PIF C2</td><td>LacIBD+PIF
-C3</td><td>LacIBD+PIF C4</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>no</td><td>no</td><td>No</td></tr>
-<tr><td>Gal4BD C1</td><td>Gal4BD C2</td><td>Gal4BD C3</td><td>Gal4BD C4</td><td>Gal4BD C5</td><td>N-Dronpa C1</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>N-Dronpa C2</td><td>N-Dronpa C3</td><td>N-Dronpa C4</td><td></td><td></td></tr>
-<tr><td>no</td><td>ok</td><td>ok</td><td></td><td></td></tr>
-</div></table>
-<p>Take glycerinated:</p>
-<ul><li>GB0030: p35S</li>
-<li>GB0036: T35S</li>
-</ul></ul>
-<ul><li>Make liquid culture of LexABD (C1-C4).</li>
-<li>We transform again LacIBD+K-Dronpa and RepBxb1:GFP, adding to the agar plates 100 µl of each transformation. </li>
-</ul></ul>
-</br><h3 style="color:green">29 June 2015</h3>
-<p>Do the minipreps of the 4 colonies of LexABD and both glycerinates, 35S and T35S.</p>
-<p>Do the digestion of the 4 colonies of LexA and both glycerinates:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexABD; pPPD2</td><td>NotI</td><td>2358, 312</td></tr>
-<tr><td>35S; pUPD2</td><td>NotI</td><td>2981, 1074</td></tr>
-<tr><td>T35S; pPUD2</td><td>NotI</td><td>2981, 304</td></tr>
-</div></table>
-<p>Make the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA C1</td><td>LexA C2</td><td>LexA C3</td><td>LexA C4</td><td>P35S</td><td>T35S</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>Ok?</td><td>Ok?</td></tr>
-</div></table>
-<p>Make ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD+K-Dronpa+promoter+termi; a1</td><td>Gal4BD+K-Donpa+prom+ter; a1</td><td>LexABD+K-Dronpa+prom+term;
-a1</td></tr>
-<tr><td>1 µl LacI, pUPD2</td><td>1 µl Gal4, pUPD2</td><td>1 µl Gal4, pUPD2</td></tr>
-<tr><td>1 µl K-Dronpa, pUPD2</td><td>1 µl K-Dronpa, pUPD2</td><td>1 µl K-Dronpa, pUPD2</td></tr>
-<tr><td>1 µl 35S (GB0030)</td><td>1 µl 35S (GB0030)</td><td>1 µl 35S (GB0030)</td></tr>
-<tr><td>1 µl T35S (GB0036)</td><td>1 µl T35S (GB0036)</td><td>1 µl T35S (GB0036)</td></tr>
-<tr><td>1.2 µl  buffer ligase</td><td>1.2 µl  buffer ligase</td><td>1.2 µl  buffer ligase</td></tr>
-<tr><td>1.2 µl BSA 10x</td><td>1.2 µl BSA 10x</td><td>1.2 µl BSA 10x</td></tr>
-<tr><td>1 µl BsaI</td><td>1 µl BsaI</td><td>1 µl BsaI</td></tr>
-<tr><td>1 µl ligase T4</td><td>1 µl ligase T4</td><td>1 µl ligase T4</td></tr>
-<tr><td>2.6 µl H2O</td><td>2.6 µl H2O</td><td>2.6 µl H2O</td></tr>
-<tr><td>1 µl a1</td><td>1 µl a1</td><td>1 µl a1</td></tr>
-<tr><td>N-Dronpa+VP16; a2</td><td>Gal4BD+PIF6; a1</td><td>LacIBD+PIF6; a1</td></tr>
-<tr><td>1 µl N-Dronpa, pUPD2</td><td>1 µl Gal4BD, pUPD2</td><td>1 µl LacIBD, pUPD2</td></tr>
-<tr><td>1 µl VP16, pUPD2</td><td>1 µl PIF6, pUPD2</td><td>1 µl PIF6, pUPD2</td></tr>
-<tr><td>1 µl 35S (GB0030)</td><td>1 µl 35S (GB0030)</td><td>1 µl 35S (GB0030)</td></tr>
-<tr><td>1 µl T35S (GB0036)</td><td>1 µl T35S (GB0036)</td><td>1 µl T35S (GB0036)</td></tr>
-<tr><td>1.2 µl  buffer ligase</td><td>1.2 µl  buffer ligase</td><td>1.2 µl  buffer ligase</td></tr>
-<tr><td>1.2 µl BSA 10x</td><td>1.2 µl BSA 10x</td><td>1.2 µl BSA 10x</td></tr>
-<tr><td>1 µl BsaI</td><td>1 µl BsaI</td><td>1 µl BsaI</td></tr>
-<tr><td>1 µl ligase T4</td><td>1 µl ligase T4</td><td>1 µl ligase T4</td></tr>
-<tr><td>2.6 µl H2O</td><td>2.6 µl H2O</td><td>2.6 µl H2O</td></tr>
-<tr><td>1 µl a2</td><td>1 µl a1</td><td>1 µl a1</td></tr>
-<tr><td>LexABD+PIF6; a1</td></tr>
-<tr><td>1 µl LexABD, pUPD2</td></tr>
-<tr><td>1 µl PIF, pUPD2</td></tr>
-<tr><td>1 µl 35S (GB0030)</td></tr>
-<tr><td>1 µl T35S (GB0036)</td></tr>
-<tr><td>1.2 µl  buffer ligase</td></tr>
-<tr><td>1.2 µl BSA 10x</td></tr>
-<tr><td>1 µl BsaI</td></tr>
-<tr><td>1 µl ligase T4</td></tr>
-<tr><td>2.6 µl H2O</td></tr>
-<tr><td>1 µl a2</td></tr>
-</div></table>
-<ul><li>Transform all the ligations into E.Coli.Gal4BD+K-Dronpa and LacIBD+K-Dronpa goes wrong and we have to do it again.
-</li>
-<li>Put into a plate the colonies before let stay them 1h at 37ºC.</li>
 </ul>
-<p>Quantification of DNA:</p>
-<ul><li>RepBxb1:GFP (C1): 163.8 ng/µl</li>
-<li>N-Dronpa, pUPD2 (C4):113.1 ng/µl</li>
-<li>N-Dronpa (C3): 83.2 ng/µl</li>
-<li>NDonpa (C1): 116.6 ng/µl</li>
-<li>Gal4BD (C1): 95.2 ng/µl</li>
-<li>Gal4BD (C2): 120.7 ng/µl</li>
-<li>RepBxb1:GFP (C2): 170.6 ng/µl</li>
-<li>RepBxb1 (C1): 80.6 ng/µl</li>
-</ul></ul>
-</br><h3 style="color:green">30 June 2015</h3>
-<p>Transform Gal4+K-Dronpa and LacI+K-Dronpa</p>
-<p>Miniprep of:</p>
-<ul><li>RepBxb1+GFP (C1-C3)</li>
-</ul></ul>
 <div class="table-wrapper"><table class="alt">
-<tr><td>RepBxb1+GFP</td><td>HindIII</td><td>6345, 2683</td></tr>
+<tr><td>20x MES MES SDS running buffer</td><td>40 ml</td></tr>
-</div></table>
+<tr><td>Distilled H<sub>2</sub>O</td><td>760 ml</td></tr>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>RepBxb1+GFP C1</td><td>RepBxb1+GFP C2</td><td>RepBxb1+GFP C3</td></tr>
-<tr><td>No</td><td>no</td><td>no</td></tr>
 </div></table>
@@ Line 1,594: / Line 431: @@
-<p>We pick more colonies and make other liquid cultures.</p>
+<p>Set aside 200 ml of 1x running buffer. Add 500 µl of NuPAGE antioxidant (only for reducing conditions). Mix by inversion.</p>
+<p>	Take one 10% Bis-Tris NuPAGE gel out of the plastic bag and rinse with distilled H<sub>2</sub>O. Peel off the white tape at the bottom of the gel.</p>
+<ul><li>Pull out the comb.</li>
-<p>Save the last samples of the leaves of the plants that were under the first experiment, next to the glycerinates in the
+<li>Insert the gel in the sure lock gel. The shorter well side of the cassettes facing inwards. Lock the gel tension wedge.</li>
-freezer (-80ºC). </p>
+<li>Fill the upper buffer chamber with the 200 ml of 1x running buffer with antioxidant. Fill  the lower buffer chamber with remaining 600 ml of 1x running buffer.</li>
-<p>Put in plates the transformations of Gal4+K-Dronpa and LacI+K-Dronpa (50 µl of bacteria in SOC medium).</p>
-<p>Make the gel:</p>
-<ul><li>Add to the digestions 2 µl of loading buffer (6x) because for 5 µl of digestion we put 1 µl of the buffer.</li>
 </ul>
-<p>Make liquid culture of two colonies for each plates of the transformations done yesterday, 10 tubes in total.</p>
+<p>To load the samples: insert the tip into the well and slowly pipet the sample into it.</p>
+<p>3.	Running the gel:</p>
+<p>Running conditions: 200 V, 40 min</p>
-<p>Take out a glycerinate 35S:Luciferase:Tnos (GB0227) and do a miniprep.</p>
+<p><b>PROTEIN TRANSFER</b></p>
-</br><h3 style="color:green">1 July 2015</h3>
+<p>1.	Preparing for transfer:</p>
-<p>Do the minipreps of the 10 liquid cultures.</p>
+<ul><li>Cut 1 piece of Hybond-P PVDF membrane and 2 pieces of whatman paper of the same size of the gel (8 x 7 cm).</li>
-<p>Do the digestions:</p>
+<li>Prepare 500 ml of  Transfer buffer:</li>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexABD+K-Dronpa;a1</td><td>EcoRI</td><td>6345, 2296</td></tr>
-<tr><td>N-Donpa+VP16; a2</td><td>HindIII</td><td>6345, 2427</td></tr>
-<tr><td>Gal4BD+PIF6; a1</td><td>EcoRI</td><td>6345, 1867</td></tr>
-<tr><td>LacI+PIF; a1</td><td>EcoRI</td><td>6345, 2638</td></tr>
-<tr><td>LexABD+PIF6; a1</td><td>EcoRI</td><td>6345, 1906</td></tr>
-</div></table>
-<p>Do the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4+PIF C1</td><td>Gal4+PIF C2</td><td>LexA+PIF C1</td><td>LexA+PIF C2</td><td>LexA+KDronpa C1</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>Ok</td></tr>
-<tr><td>LexA+Kdronpa C2</td><td>LacI+PIF C1</td><td>LacI+PIF C2</td><td>Ndonpa+VP16 C1</td><td>Ndronpa+VP16 C2</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td></tr>
-</div></table>
-<ul><li>Prepare liquid culture of:</li>
 </ul>
-<ul><li>LexA+PIF; ?1 (C1)</li>
-<li>LacI+PIF; ?1 (C1)</li>
-<li>LexA+K-Dronpa (C1)</li>
-<li>Gal4+PIF; ?1 (C1)</li>
-<li>VP16, pUPD2 (C1)</li>
-<li>LexABD, pUPD2 (C2)</li>
-<li>PIF6, pUPD2 (C5)</li>
-<li>LacIBD, pUPD2 (C1)</li>
-</ul></ul>
-<ul><li>Pick colonies and make liquid culture of:</li>
-<ul class="ul_2"><li>Gal4+K-Dronpa (C1 and C2)</li>
-<li>LacI+K-Dronpa (C1 and C2)</li>
-<li>RepBxb1+GFP (C4-C6)</li>
-</ul><li>We sent to sequence:</li>
-<ul class="ul_2"><li>Code:</li>
-<li>210.08-249: pUPD2, KDronpa C3</li>
-<li>210.08-250: pUPD2, NDronpa C1</li>
-<li>210.08-251: pUPD2, NDronpa C3</li>
-<li>210.08-252: pUPD2, NDronpa C4</li>
-<li>The solution have: 10µl of miniprep + 5µl (dilution 1:3) of primers.</li>
-</ul></ul>
-<ul><li>Data of the luciferase essay with the sample plat RED at 24h (replica2): we obtain a value of 7.4E6.</li>
-</ul>
-</br><h3 style="color:green">2 July 2015</h3>
-<p>Minipreps of:</p>
-<ul><li>Gal4+K-Dronpa (C1 and C2)</li>
-<li>LacI+K-Dronpa (C1 and C2)</li>
-<li>RepBxb1+GFP (C4-C6)</li>
-</ul></ul>
 <div class="table-wrapper"><table class="alt">
-<tr><td>Gal4+K-Dronpa</td><td>EcoRI</td><td>6345, 3028</td></tr>
+<tr><td>Transfer buffer (x20)</td><td>25 ml</td></tr>
-<tr><td>LacI+K-Dronpa</td><td>EcoRI</td><td>6345, 2257</td></tr>
+<tr><td>Methanol</td><td>50 ml</td></tr>
-<tr><td>RepBxb1+GFP</td><td>HindIII</td><td>6300, 2400</td></tr>
+<tr><td>H<sub>2</sub>O</td><td>375 ml</td></tr>
 </div></table>
@@ Line 1,738: / Line 473: @@
-<p>Do the gel:</p>
+<ul><li>Soak 5 blotting pads in transfer buffer. Remove air bubbles by squeezing the blotting pads while they are submerged in buffer (this step is important because air bubbles may block the transfer of proteins).</li>
+<li>Pre-wet the PVDF membrane for 10’’ in methanol. Wash in distilled water for 5’. Equilibrate in transfer buffer for at least 10’ before blotting. (Everything is done without agitation).</li>
+<li>Wathman paper: soak briefly in transfer buffer immediately before using.</li>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI+K-Dronpa C1</td><td>LacI+K-Dronpa C2</td><td>Gal4+K-Dronpa C1</td><td>Gal4+K-Dronpa C2</td></tr>
-<tr><td>??</td><td></td><td></td></tr>
-<tr><td>RepBxb1+GFP C4</td><td>RepBxb1+GFP C5</td><td>RepBxb1+GFP C6</td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-</div></table>
-<p>Luciferase essay: </p>
-<ul><li>During the whole experiment we lost three samples: T16/FarRed/1; T24/Red/2 and T0/FarRed/1</li>
 </ul>
-<p>Results:</p>
+<ul><li>Lay the gel on the bench allowing one edge to hang 1 cm over the side. Insert the gel-knife into the gap between the gel plates and push up and down gently to break the bonds that hold the plates together. When all the bonds are broken separate the two plates and throw away the one without the gel.</li>
-<p>Things to keep in mind for the next experiment:</p>
+<li>Cut the wells with the gel-knife.</li>
-<ul><li>The luminimeter (machine to measure the luminescence) has to be ready before start adding the reactants to the
+<li>Place a piece of pre-soaked whatman paper on top of the gel. Keep the filter paper saturated with transfer buffer and remove all trapped air bubbles by gently rolling a glass pipette over the surface.</li>
-samples because it needs 10min to be ready.</li>
+<li>Turn the plate over so that the gel and whatman paper are facing downwards over your hand or over a piece of parafilm on the bench. </li>
-<li>Set the timer (10min) with the first sample of luciferase and add the reactant to the other samples as quick as
+<li>Remove the gel from the plate: use the gel knife to carefully loosen the bottom of the gel so that it peels away from the plate.</li>
-possible. </li>
-<li>We have to let the renilla stay before putting it in the luminimeter the same time as the luciferase, in this case
-min because with the luciferase we didn’t manage well the time. Theoretically we have to wait 10min.</li>
-</ul></ul>
-<p>Make ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:Kdonpa+N-Dronpa; ?1</td><td>LacI:Kdronpa+N-Dronpa; ?1</td><td>Gal4:Kdronpa+N-Dronpa; ?1</td></tr>
-<tr><td>1 µl LexA:Kdronpa</td><td>1 µl LacI:Kdronpa</td><td>1 µl Gal4:Kdronpa</td></tr>
-<tr><td>1 µl N-Dronpa</td><td>1 µl N-Dronpa</td><td>1 µl N-Dronpa</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl BsaI</td><td>1 µl BsaI</td><td>1 µl BsaI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>LexA:PIF+PhyB:VP16; ?1</td><td>LacI:PIF+PhyB:VP16; ?1</td><td>Gal4:PIF+PhyB:VP16; ?1</td></tr>
-<tr><td>1 µl LexA:PIF</td><td>1 µl LacI:PIF</td><td>1 µl Gal4:PIF</td></tr>
-<tr><td>1 µl PhyB:VP16 (88E)</td><td>1 µl PhyB:VP16</td><td>1 µl PhyB:VP16</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl BsaI</td><td>1 µl BsaI</td><td>1 µl BsaI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>35S:Bxb1+RepBxb1:GFP; ?1</td><td>E-PIF+phyB+luc+ren; ?1</td></tr>
-<tr><td>1 µl 35s:Bxb1:T35S (alfredo’s)</td><td>0.5 µl 896 (PIF+phy+luc)</td></tr>
-<tr><td>1 µl PromsinATG:RepBxb1:GFP</td><td>1 µl 160 (renilla)</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl BsaI</td><td>1 µl BsaI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-<p>The samples that we sent to sequence have arrived:</p>
-<ul><li>210.08-249: pUPD2, KDronpa C3------ok</li>
-<li>210.08-250: pUPD2, NDronpa C1------ok</li>
-<li>210.08-251: pUPD2, NDronpa C3------ok</li>
-<li>210.08-252: pUPD2, NDronpa C4------ok</li>
-</ul></ul>
-<p>The sequences of N-Dronpa have the desired mutation.</p>
-<ul><li>Transformation in E.Coli of the 8 ligations.</li>
-<li>Put the transformation into plates, put at 37ºC.</li>
-<li>Refresh the Agro’s cultures (Renilla and PIF+phy+luc):</li>
-<li>Add in 5ml of LB, 5 µl of rifampicine, 5 µl kanamicine, 5 µl of culture.</li>
 </ul>
-</br><h3 style="color:green">4 July 2015</h3>
+<p>3.	Transferring the gel: </p>
+<ul><li>Wet the surface of the gel with transfer buffer and place a pre-soaked membrane on top of the gel. Make a small cut on one corner of the membrane to mark the orientation. Remove air bubbles by rolling a glass pipette over the membrane surface.</li>
+<li>Place a pre-soaked whatman paper on top of the membrane. Remove air bubbles.</li>
-<p>Make the 2nd refresh of the culture of <i>Agrobacterium</i>. Put 5ml of LB, 5 µl of rifampicine, 5 µl kanamicine, 5 µl
+<li>Place 2 soaked blotting pads into the Xcell II Blot Module. Place the paper-gel-membrane-paper sandwich on top of the blotting pads.</li>
-of culture.</p>
+<li>Add another 3 pre-soaked blotting pad on top of the sandwich.</li>
+<li>Place the blot module in the buffer chamber. Lock the gel tension wedge into place.</li>
+<li>Fill the blot module with transfer buffer until the gel-membrane sandwich is covered in buffer (do not fill all the way to the top as this generates extra conductivity and heat).</li>
-<p>Make liquid cultures (4ml of LB and 4 µl of spectomicine) of the 8 colonies of E.Coli. </p>
+<li>Fill the outer buffer chamber with ˜ 650 ml deionized water. </li>
-<ul><li>Red toggle (C1)</li>
+<li>Running conditions: 30V for 2h</li>
-<li>Gal4:Kdronpa+N-Dronpa (C1 and C2)</li>
-<li>LexA:Kdonpa+N-Dronpa (C1 and C2)</li>
-<li>LacI:Kdronpa+N-Dronpa (C1 and C2)</li>
-<li>LexA:PIF+PhyB:VP16 (C1 and C2)</li>
-<li>35S:Bxb1+RepBxb1:GFP (C1 and C2)</li>
-<li>This colonies didn’t grow: LacI:PIF+PhyB:VP16; Gal4:PIF+PhyB:VP16 and E-PIF+phyB+luc+ren. Tomorrow we will repeat the
-ligations.</li>
-</ul></ul>
-</br><h3 style="color:green">5 July 2015</h3>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:PIF+PhyB:VP16; ?1</td><td>Gal4:PIF+PhyB:VP16; ?1</td></tr>
-<tr><td>1 µl LacI:PIF</td><td>1 µl Gal4:PIF</td></tr>
-<tr><td>1 µl PhyB:VP16</td><td>1 µl PhyB:VP16</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>1.2 µl buffer ligase</td><td>1.2 µl buffer ligase</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>4.6</td><td>µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-<p>Minipreps of the liquid cultures.</p>
-<p>Digestion of the minipreps.</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:Kdronpa+N-Dronpa</td><td>BamHI</td><td>6674, 5437</td></tr>
-<tr><td>35S:Bxb1+RepBxb1:GFP</td><td>BamHI</td><td>6674, 3859, 1782</td></tr>
-<tr><td>Gal4:Kdronpa+N-Dronpa</td><td>BamHI</td><td>6674, 4666</td></tr>
-<tr><td>LexA:Kdonpa+N-Dronpa</td><td>BamHI</td><td>6674, 4705</td></tr>
-<tr><td>LexA:PIF+PhyB:VP16</td><td>BamHI</td><td>6674, 3513, 2337</td></tr>
-</div></table>
-<ul><li>Agarose gel (1%): </li>
 </ul>
-<div class="table-wrapper"><table class="alt">
+<p><b>BLOCKING THE MEMBRANE</b></p>
-<tr><td>LacKN C1</td><td>LacIKN C2</td><td>Bxb1RepGFP C1</td><td>Bxb1RepGFP C2</td><td>Gal4KN C1</td><td>Gal4KN
+<p>1.	Prepare 50 ml of blocking solution.</p>
-C2</td></tr>
+<p>2% ECL Advance Blocking Agent in PBS-T (pH 7.5):</p>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>LexA:KN C1</td><td>LexA:KN C2</td><td>LexAPIFPhy C1</td><td>LexAPIFPhy C2</td><td>Red toggle</td><td></td></tr>
-<tr><td>ok</td><td>ok</td><td>no</td><td>no</td><td>no</td><td></td></tr>
+<ul><li>1 g blocking agent</li>
-</div></table>
+<li>50 ml PBS (1x)</li>
+<li>50 µl Tween-20</li>
-<p>We have to repeat the digestion of: LexA+PIF:phy+VP16.</p>
-<ul><li>Take out the glycerinate 88C (1098): Etr8:luc:Tnos. We will use it like a negative control in the second
-luciferase essat.</li>
-<li>Calculation of the ODs:</li>
-<ul class="ul_2"><li>Dilution of both samples 1:10.</li>
-<li>Renilla:=0.22---182 µl of sample + 1.818 ml MES</li>
-<li>PIF+PhyB+Luc=0.26--- 154 µl of sample + 1.646 ml MES</li>
 </ul></ul>
-<p>Agroinfiltration of the two samples with renilla and luciferase+PIF+phy in three plants with 4 spots in each leaf and 2
+<p>2.	Take the membrane out of the blotting module and transfer it to the blocking solution (protein side up, work always this way from now on). Leave o/n at 4ºC.</p>
-leaf in each plant.</p>
-<p>Let the plants 2 days in the darkness till agrobacterium infects the plant. They have to be in the dark because we are
-trying our red toggle ant it activates with light.</p>
+<p><b><u>DAY 2</u></b></p>
+<p><b>DETECTION</b></p>
-</br><h3 style="color:green">6 July 2015</h3>
+<p>1.	Prepare 2 L of  wash buffer (PBS-0.1% Tween (pH 7.5))</p>
-<p>Transform the negative control into agrobacterium.</p>
+<ul><li>200 ml PBS 5x (pH 7.5)</li>
-<ul><li>Etr8:luc:Tnos</li>
+<li>800 ml distilled H<sub>2</sub>O</li>
-<li>Bxb1:reporterBxb1:GFP</li>
+<li>1 ml Tween 20</li>
 </ul></ul>
-<p>We were doing dry lab preparing the power point to present our project to the rector and biotecs companies.</p>
+<p>3.	Prepare 10 ml of antibody diluent (2% ECL Advance blocking agent in PBS-0.1%Tween) for each antibody you are going to use.</p>
+<p>4.	For 6x His-tag detection: dilute the Anti-His6 mouse monoclonal antibody 1:2000 in 10 ml of antibody diluent (5 µl antibody in 10 ml antibody diluent).  Incubate for 1h at RT on a shaker.</p>
+<p>For IgA detection: dilute the Anti-IgaH antibody 1:20000 in 10 ml of antibody diluent (0.5 µl antibody in 10 ml antibody diluent).  Incubate for 1h at RT on a shaker. This antibody is already conjugated to HRP and does not need a secondary antibody for detection; go directly to step 8 after the 1 incubation.</p>
-</br><h3 style="color:green">7 July 2015</h3>
+<p>5.	Discard the antibody solution and wash the membrane with wash buffer:</p>
-<p>Luciferase essay: Copy the protocol.</p>
+<ul><li>2 x brief wash</li>
-<ul><li>Add 150 µl of the lisis buffer and 800µl of MiliQ water, dilution 1:5.</li>
+<li>1 x 15’ wash (RT, shaker)</li>
-<li>We centrifuge both cultures of agrobacterium at 2900rpm for 10min and remove the supernatant. </li>
+<li>3 x 5’ wash (RT, shaker)</li>
-<li>We prepare the stock of MES (10ml of MES + 1ml MgCl + 100µl of “Acetosiningona” and level with H2O until 100ml.</li>
-<li>Resuspend the pellet of bacteria with 5ml of MES and let grow 2h.</li>
-</ul></ul>
-<ul><li>Renilla=0.29 (dilution 1:10): 2.9</li>
-<li>PhyB+PIF+luc=0.69 (dilution 1:4):2.76</li>
-<li>Solution to agroinflitrate:</li>
-<li>Renilla: 0.138ml of sample + 1.862ml of MES</li>
-<li>PhyB+PIF+luc: 0.145ml of sample + 1.855ml of MES</li>
-<li>We make the infiltration of both samples mix together in 3 different plants, 2 leaf per plant and 4 spots per leaf.
-Explicacion del experiment (tiempo en oscuridad… luces…)</li>
-</ul></ul>
-<p>Digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Red toggle</td><td>Enzyme?</td><td></td></tr>
-<tr><td>LexA+PIF+phy</td><td>BamHI</td><td>3518, 5855, 6674</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Red toggle</td><td>LexA+PIF+phy C1</td><td>LexA+PIF+phy C2</td></tr>
-<tr><td>No</td><td>Ok</td><td>no</td></tr>
-</div></table>
-<p>It has arrived a new construction: AsLOVpep.</p>
-<ul><li>Suspended with 50µl of H2O.</li>
-</ul></ul>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>AsLOVpep; pUPD2</td><td>Red Toggle</td><td>LacI:Kdronpa:Ndronpa:VP16+</td></tr>
-<tr><td>35S:renilla:Tnos-35S:P19:Tnos(GB159)</td><td>Gal4:Kdronpa:Ndronpa:VP16+GB159</td></tr>
-<tr><td>1 µl AsLOVpep</td><td>1 µl GB846</td><td>1 µl LacI:KNdronpa:VP16</td><td>1 µl Gal4:KNdronpa</td></tr>
-<tr><td>1 µl pUPD2</td><td>1 µl GB160</td><td>1 µl GB159</td><td>1 µl GB159</td></tr>
-<tr><td>1.2 µl buffer</td><td>1 µl ?1</td><td>1 µl a1</td><td>1 µl a1</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1 µl BsmbI</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>5.6 µl H2O</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td></td><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>LexA:Kdronpa:Ndronpa:VP16+GB159</td><td>LexA:PIF:Phy:VP16+ GB159</td></tr>
-<tr><td>1 µl LexA:Kdronpa:Ndronpa:VP16</td><td>1 µl LexA:PIF:Phy:VP16</td></tr>
-<tr><td>1 µl GB159</td><td>1 µl GB159</td></tr>
-<tr><td>1 µl a1</td><td>1 µl a1</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-</br><h3 style="color:green">8 July 2015</h3>
-<ul><li>Experiment to study the piece PhyB+PIF.</li>
 </ul>
-<p>	The plants in red are exposed at the light intensity of the leds (we can’t regulate it) and the plants in far red
+<p>7.	Incubate the membrane with the secondary antibody for 1h at RT on a shaker.</p>
-are 100% with far red light and 0% of white light.</p>
+<p>8.	Repeat step 5.</p>
-<p>	How the machines work: (hace falta?)</p>
+<p>9.	Take the detection reagents from the fridge and allow to equilibrate to RT before opening.</p>
-<p>	The machine with red light has the switch …</p>
+<p>10.	Mix detection solutions ECL Plus A and B in a ratio 40:1. </p>
-<p>	The 1st sample its at 8:00am and we spend 1h till the machines were working correctly because we didn’t know
+<p>	975 µl Sol. A + 25 µl Sol. B (enough for 1 membrane)</p>
-exactly how they work.</p>
+<p>11.	Drain the excess wash buffer from the membrane by holding the membrane gently with forceps and touching the edge against a tissue. Place the membrane protein side up on an acetate sheet. Pipette the mixed detection reagent on to the membrane. </p>
-<p>	Then, before 12h (21:00), we take the 2nd samples; obtainin 3 discs of each condition (red an far red). </p>
+<p>12.	Cover the membrane with another acetate sheet and gently smooth out any air bubbles, but do not apply pressure over the membrane. Dry any extra liquid with tissue.</p>
+<p>13.	Place a piece of filter paper on a X-ray film cassette (fix with tape). Drain excess of detection solution with a tissue and place the wrapped blots on top of the paper (fix with tape). Close the cassette and take to the dark room together with the autoradiography films and timer.</p>
+<p>14.	Switch on the film processor (front panel, lower right corner). Check that the temperate selector on top of the switch on button is on position 2. Turn off the light and with the red light on open the cassette and place a sheet of autoradiography film on top of the membrane (bend the lower right corner to mark the orientation). Close the cassette and expose the film for 1’. To develop the film place it on the rear feeding tray (shorter side of the film opposite to the bent corner against the feeding area to minimize the possibility that the film gets stack in the processor) and press the button next to it to start the feeding. Adjust exposure time as necessary.</p>
+				    	</p><br/>
+				    </div>
+				</details>
+				<details>
+				    <summary class="button fit">Protoplasts protocol</summary>
+				    <div class="clsPadding">
+				    	<p><p>We make protoplasts in to different ways. At first we make protoplasts with a normal Nicotiana leaf and then we try to transform the alive protoplasts. After the infiltration at vacuum we can not obtain protoplasts, we change the method. First we agroinfiltrate leafs with the desired construction, we let them 3 hours in dark and then make the protoplasts. The general steps for every preparation is:</p>
-<p>We transform:</p>
+<p>1.	Prepare the enzymatic solution. It has 5mL of Mannitol (0.8M) + 200 µl KCl (1M) + 400 µl MES (0.5M, pH 5.7) + 150ng cellulase + 40mg Macerozyme + 4.2mL H<sub>2</sub>O. Total volume for one preparation. Put it 10min at 55ºC. </p>
-<ul><li>AsLOVpep; pUPD2 in DHSa an let incubate 1h at 37ºC.</li>
+<p>2.	Take out the solution and let it cool down.</p>
-<li>The last ligations in E.coli. Put in plates. Red toggle with Spectomicine+IPTG+XGal ann the rest (a1) with kanamicine
+<p>3.	Add 100 µl CaCl<sub>2</sub> + 4 µl Beta-Mercaptoethanol + 100 µl BSA (10%).</p>
-+IPTG+XGal.</li>
+<p>4.	Put the enzymatic solution in a petri dish and cut the leaf in very thin strips. Put quickly the cut leafs so they do not dry.</p>
-</ul></ul>
+<p>5.	In darkness, do the vacuum for 30min to the petri dish with the enzymatic solution and the cut leaf. Let the leaf 3h in darkness, no agitation.</p>
-</br><h3 style="color:green">9 July 2015</h3>
+<p>6.	Swirl the plate gently. Using a 5ml pipette tip (cut off the tip first) take the liquid and filter them with a 35-75 µm nylon mesh into a 13 mL tube. To clean the mesh add before a little bit of W5 solution. Also put the leaf stripes first and then throw the enzymatic solution.</p>
+<p>7.	Add 5ml of W5 solution.</p>
+<p>8.	Centrifuge at 100xg for 1min without brake.</p>
-<p>Pick colonies:</p>
+<p>9.	Eliminate the supernatant. Leave a small volume so that the protoplasts do not dry.</p>
-<ul><li>AsLOVpep colonies didn’t grow. Repeat.</li>
+<p>10.	Add WI solution till reach the desired concentration (10<sup>7</sup> protoplasts per gram). </p>
-<li>Red toggle colonies are all blue. Repeat.</li>
+<p>11.	Finally put into the plate wells 250 µl of W5 and 100 µl of protoplasts solution.</p>
-<li>The other 4 colonies had grown. we pick them and male liquid culture.</li>
+<p>Solutions:</p>
-<li>LacI:Kdronpa:Ndronpa:VP16+renilla (C1-C3)</li>
+<p>W5: NaCl (154mM) + CaCl<sub>2</sub> (125mM) + KCl (5mM) + MES (2mM) + 17.8ml H20. Total volume of 50ml.</p>
-<li>Gal4:Kdronpa:Ndronpa:VP16+renilla (C1-C3)</li>
+<p>WI: MES (4mM)(pH 5.7) + NaCl (154mM) + CaCl<sub>2</sub> (20mM).</p>
+				    	</p><br/>
+				    </div>
+				</details>
+				<details>
+				    <summary class="button fit">Protoplast luciferase assay protocol</summary>
+				    <div class="clsPadding">
+				    	<p><p>Before doing the essay the protoplasts are in a plate in the light conditions needed.</p>
-<li>LexA:Kdronpa:Ndronpa:VP16+GB159 (C1 and C2)</li>
+<p>1.	Take the solution with protoplasts and put it in an Eppendorf.</p>
-<li>LexA:PIF:Phy:VP16+ GB159 (C1 and C2)</li>
+<p>2.	Centrifugue at 100xg for 1min.</p>
-</ul></ul>
+<p>3.	Eliminate the maximum supernatant letting the protoplasts.</p>
-<p>Repeat the ligations.</p>
+<p>4.	Put into liquid nitrogen and then keep it in the -80ºC fridge.</p>
-<ul><li>AsLOVpep, as before.</li>
+<p>Start the essay:</p>
-</ul></ul>
+<p>5.	Add to the freeze sample 100µl of Passive lysis buffer (1x).</p>
-<div class="table-wrapper"><table class="alt">
+<p>6.	Vortex the samples.</p>
-<tr><td>Red toggle (PIF+PhyB+luc+ren)</td></tr>
+<p>7.	Let it 5min in ice.</p>
-<tr><td>0.5 µl PIF+phy+luc (896)</td></tr>
+<p>8.	Centrifuge it at 1000xg for 2min.</p>
-<tr><td>1 µl renilla (160)</td></tr>
+<p>9.	Eliminate the supernatant.</p>
-<tr><td>1 µl ?1</td></tr>
+<p>10.	Take an opaque plate to measure the luciferase and put in each well 40 µl of Luciferase and 10 µl of sample, wait 10min and then measure.</p>
-<tr><td>1.2 µl buffer</td></tr>
+<p>11.	Add to the wells 40 µl of Dual Glo (1x) and measure the renilla luminiscence.</p>
-<tr><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl BsmbI</td></tr>
-<tr><td>1 µl T4 ligase</td></tr>
-<tr><td>5.1 µl H2O</td></tr>
-</div></table>
-<p>We do the luciferase essay:</p>
-<ul><li>We didn’t obtain goo results, we can’t observed a significative difference between the on(red samples) and off
-(far red samples). It seems that the red toggle it has been activated. Graphics and tables</li>
-</ul></ul>
-<p>Transform the ligations of AsLOVpepe and red toggle. </p>
-<ul><li>Add SOC medium and let incubate 1h at 37ºC. Then we make an spin to the red toggle cells to concentrate them and
-see if we can obtain a colonies in the plates.</li>
-</ul></ul>
-</br><h3 style="color:green">10 July 2015</h3>
-<p>Minipreps of:</p>
-<ul><li>LexABD:PIF:phyB:VP16+Renilla; a1 (C1,C2)</li>
-<li>LexA:Kdronpa:Ndronpa+renilla; a1C1, C2)</li>
-<li>Gal4:Kdronpa:Ndronpa+renilla; a1 (C1-C3)</li>
-<li>LacI:Kdronpa:Ndronpa+renilla; a1 (C1,C2)</li>
-</ul></ul>
-<p>Digestions of:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexABD:PIF:phyB:VP16+Renilla; a1 (C1,C2)</td><td>EcoRI</td><td>6345, 5487, 4891</td></tr>
-<tr><td>LexA:Kdronpa:Ndronpa+renilla; a1C1, C2)</td><td>EcoRI</td><td>9333, 6345</td></tr>
-<tr><td>Gal4:Kdronpa:Ndronpa+renilla; a1 (C1-C3)</td><td>EcoRI</td><td>6345, 9194</td></tr>
-<tr><td>LacI:Kdronpa:Ndronpa+renilla; a1 (C1,C2)</td><td>EcoRI</td><td>6345, 9965</td></tr>
-<tr><td>LacIBD+PIF+phyB; &Omega;1 (C1)</td><td>BamHI</td><td>6674, 4245, 2337</td></tr>
-<tr><td>Gal4BD+PIF+phyB; &Omega; 1 (C1)</td><td>BamHI</td><td>6674, 3474, 2337</td></tr>
-</div></table>
-<p>Make the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacIBD+PIF+phyB</td><td>Gal4BD+PIF+phyB</td><td>LexA:PIF:phyB:VP16+Renilla C1</td><td>LexA:PIF:phyB:VP16+Renilla
-C2</td></tr>
-<tr><td>Ok</td><td>Ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>LexA:KNdronpa+renilla C1</td><td>LexA:KNdronpa+renilla C2</td><td>Gal4:KNdronpa+renilla C1</td><td>Gal4:KNdronpa
-+renilla C2</td></tr>
-<tr><td>Ok</td><td>Ok</td><td>ok</td><td>Ok</td></tr>
-<tr><td>Gal4:KNdronpa+renilla C3</td><td>LacI:Kdronpa:Ndronpa+renilla C1</td><td>LacI:Kdronpa:Ndronpa+renilla
-C2</td><td></td></tr>
-<tr><td>Ok</td><td>Ok</td><td>ok</td><td></td></tr>
-</div></table>
-<p>We received two constructions:</p>
-<ul><li>CDS: phiC31. Resuspended with 100µl.</li>
-<li>Reporter phi31. Resuspended with 50 µl</li>
-</ul></ul>
-<p>Pick colonies and make liquid culture of:</p>
-<ul><li>AsLOVpep; pUPD2 (C1 and C2)</li>
-<li>Red toggle (C1 and C2). In both liquid cultures we ad YPTG and Xgal to make sure that the colonies are correct, if not
-the medium will change to blue color.</li>
-</ul></ul>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2</td><td>Reporter phiC31; pUPD2</td><td>LacI:PIF:Phy:VP16+ren; a1</td></tr>
-<tr><td>1 µl phiC31</td><td>1 µl rep phiC31</td><td>1 µl LacI:PIF:Phy:VP16</td></tr>
-<tr><td>1 pUPD2</td><td>1 pUPD2</td><td>1 µl renilla (159)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td><td>1 µl BSAI</td></tr>
-<tr><td>5.6 µl H2O</td><td>5.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td></td><td>1 µl a1</td></tr>
-<tr><td>Gal4:PIF:phy:VP16+ren; a1</td><td>LexA:PIF:phy:ren+opLex:luc; ?1</td><td>LexA:KNdronpa:ren+OpLex:Luc; ?1</td></tr>
-<tr><td>1 µl Gal4:PIF:phy:VP16</td><td>1 µl LexA:PIF:phy:ren</td><td>1 µl LexA:KNdronpa:ren</td></tr>
-<tr><td>1 µl renilla (159)</td><td>1 µl opLex:luc (151)</td><td>1 µl OpLex:Luc (151)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA </td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BSAI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>1 µl a1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>Gal4:KNdronpa:ren+UAS:luc; ?1</td><td>LacI:KNdronpa:ren+OpLacI:luc; ?1</td></tr>
-<tr><td>1 µl Gal4:KNdronpa:ren</td><td>1 µl LacI:KNdronpa:ren</td></tr>
-<tr><td>1 µl UAS:luc (227)</td><td>1 µl OpLacI:luc (152)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA </td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-</div></table>
-</br><h3 style="color:green">11 July 2015</h3>
-<p>Prepare glycerinates of:</p>
-<ul><li>Bxb1+Rep:GFP; ?1</li>
-<li>N-Dronpa; pUPD2</li>
-<li>Bxb1:Etr8; pUPD2</li>
-<li>Etr8(CMV):Bxb1:T35S; a1</li>
-</ul></ul>
-<p>Pick up the liquid cultures of AsLOVpep and red toggle. We observed that one tube of a red toggle colony is blue, we
-discard it.</p>
-<p>Do miniprep of:</p>
-<ul><li>AsLOVpep (C1 and C2)</li>
-<li>Red toggle (C2)</li>
-</ul></ul>
-<p>Digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Red toggle</td><td>BamHI</td><td>6674, 6100 / 4209, 3756</td></tr>
-<tr><td>AsLOVpep</td><td>NotI</td><td>2558, 512</td></tr>
-</div></table>
-<p>Me falta el resultado del gel!!</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>AsLOVpep C1</td><td>AsLOVpep C2</td><td>Red toggle C2</td></tr>
-<tr><td>¿?</td><td></td></tr>
-</div></table>
-<p>Do transformation of DHSa and yesterday ligations:</p>
-<ul><li>phyC31;pUPD2</li>
-<li>Reporter phiC31; pUPD2</li>
-<li>LacI:PIF:Phy:VP16+ren; a1</li>
-<li>Gal4:PIF:phy:VP16+ren; a1</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1</li>
-<li>LexA:KNdronpa:ren+OpLex:Luc; ?1</li>
-<li>Gal4:KNdronpa:ren+UAS:luc; ?1</li>
-<li>LacI:KNdronpa:ren+OpLacI:luc; ?1</li>
-<li>The pUPD2 in plates with cloranfenicol+IPTG+XGal. The a1 in plates with kanamicyn+IPTG+XGal. The ?1 in plates with
-spectinmicyn+IPTG+XGal.</li>
-</ul></ul>
-</br><h3 style="color:green">12 July 2015</h3>
-<p>Pick colonies and make liquid culture:</p>
-<ul><li>phyC31;pUPD2 (C1-C3)</li>
-<li>Reporter phiC31; pUPD2 (C1-C3)</li>
-<li>LacI:PIF:Phy:VP16+ren; a1 (C1-C3)</li>
-<li>Gal4:PIF:phy:VP16+ren; a1  All blue colonies.</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1 (C1)</li>
-<li>LexA:KNdronpa:ren+OpLex:Luc; ?1(C1-C3)</li>
-<li>Gal4:KNdronpa:ren+UAS:luc; ?1 (C1)</li>
-<li>LacI:KNdronpa:ren+OpLacI:luc; ?1 All blue colonies.</li>
-<li>We have to repeat the transformations or do again ligations.</li>
-</ul></ul>
-<p>Ligations were repeated:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4:PIF:phy:VP16+ren; a1</td><td>LacI:KNdronpa:ren+OpLacI:luc; ?1</td></tr>
-<tr><td>1 µl Gal4:PIF:phy:VP16</td><td>1 µl LacI:KNdronpa:ren</td></tr>
-<tr><td>1 µl renilla (159)</td><td>1 µl OpLacI:luc (152)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA </td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BSAI</td><td>1 µl BsmbI</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>1 µl a1</td><td>1 µl ?1</td></tr>
-</div></table>
-<p>Refresh the liquid cultures of <i>Agrobacterium</i>:</p>
-<ul><li>Bxb1:GFP and Etr8:tnos. They were 2 days at 28ºC.</li>
-<li>Pnos, it was at the fridge (-4ºC).</li>
-</ul></ul>
-</br><h3 style="color:green">13 July 2015</h3>
-<p>All the liquid cultures have grown, do minipreps.</p>
-<p>Do digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2 (C1-C3)</td><td>NotI</td><td>2046, 1899</td></tr>
-<tr><td>Reporter phiC31; pUPD2 (C1-C3)</td><td>NotI</td><td>2046, 475</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren; a1 (C1-C3)</td></tr>
-<tr><td></td><td>EcoRI</td><td>6345, 5623, 5487</td></tr>
-<tr><td>LexA:PIF:phy:ren+opLex:luc; ?1 (C1)</td></tr>
-<tr><td></td><td>BamHI</td><td>9431, 6674, 3531</td></tr>
-<tr><td>LexA:KNdronpa:ren+OpLex:Luc; ?1(C1-C3)</td></tr>
-<tr><td></td><td>BamHI</td><td>1199, 6674</td></tr>
-<tr><td>Gal4:KNdronpa:ren+UAS:luc; ?1 (C1)</td></tr>
-<tr><td></td><td>BamHI</td><td>11582, 6674</td></tr>
-</div></table>
-<p>Agarose gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31 C1</td><td>phyC31 C2</td><td>phyC31 C3</td><td>RepPhiC31 C1</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>ok</td></tr>
-<tr><td>RepPhiC31 C2 </td><td>LacI:PIF:Phy:VP16+ren C1</td><td>LacI:PIF:Phy:VP16+ren C2</td><td>LacI:PIF:Phy:VP16+ren
-C3</td></tr>
-<tr><td>no</td><td>no</td><td>ok</td><td>ok</td></tr>
-<tr><td>LexA:PIF:phy:ren+opLex:luc</td><td>LexA:KNdronpa:ren+OpLex:Luc C1</td><td>LexA:KNdronpa:ren+OpLex:Luc
-C2</td><td>LexA:KNdronpa:ren+OpLex:Luc C3</td></tr>
-<tr><td>no</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>Gal4:KNdronpa:ren+UAS:luc C1</td><td></td><td></td></tr>
-<tr><td>no</td><td></td><td></td></tr>
-</div></table>
-<p>The <i>Agrobacterium</i> cultures refreshed yesterday were store in the fridge.</p>
-<p>It is made another culture of 35S:Bxb1+reporterBxb1:GFP to keep it in the fridge. It had 5ml of LB medium, 5 µl
-rifampicin and 5 µl of spectinomicyn an 1 µl of the culture. </p>
-<p>Mesurement of the OD’s:</p>
-<ul><li>35S:Bxb1+reporterBxb1:GFP: 0.28 (dilution 1:10)</li>
-<li>143 µl of culture+1857 µl of MES/acetosiningon solution.</li>
-<li>With this preparation 2 plants were infiltrated and let in natural light to see the normal activity of the
-recombinase.</li>
-</ul></ul>
-<p>Transformation of the ligation: Gal4:PIF:phy:VP16+ren; a1 and LacI:KNdronpa:ren+OpLacI:luc; ?1.</p>
-<p>The liquid cultures of this constructions were repeated:</p>
-<ul><li>phyC31;pUPD2 (C4 and C5)</li>
-<li>Reporter phiC31; pUPD2 (C4)</li>
-<li>LacI:PIF:Phy:VP16+ren; a1 (C4)</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1 (C1)</li>
-<li>LexA:KNdronpa:ren+OpLex:Luc; ?1(C1-C3)</li>
-<li>Gal4:KNdronpa:ren+UAS:luc; ?1 (C1)</li>
-<li>AsLOVpep; pUPD2 (C3)</li>
-</ul></ul>
-</br><h3 style="color:green">14 July 2015</h3>
-<p>Do minipreps of:</p>
-<ul><li>phyC31;pUPD2 (C4 and C5)</li>
-<li>Reporter phiC31; pUPD2 (C4)</li>
-<li>LacI:PIF:Phy:VP16+ren; a1 (C4)</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1 (C1)</li>
-<li>LexA:KNdronpa:ren+OpLex:Luc; ?1(C1-C3)</li>
-<li>Gal4:KNdronpa:ren+UAS:luc; ?1 (C1)</li>
-<li>AsLOVpep; pUPD2 (C3)</li>
-</ul></ul>
-<p>Do digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2</td><td>NotI</td><td>2046, 1899</td></tr>
-<tr><td>Reporter phiC31; pUPD2</td><td>NotI</td><td>2046, 475</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren; a1</td><td>EcoRI</td><td>6345, 5623, 5487</td></tr>
-<tr><td>LexA:PIF:phy:ren+opLex:luc, ?1</td><td>BamHI</td><td>9431, 6674, 3531</td></tr>
-<tr><td>LexA:KNdronpa:ren+OpLex:Luc; ?1</td><td>BamHI</td><td>1199, 6674</td></tr>
-<tr><td>Gal4:KNdronpa:ren+UAS:luc; ?1</td><td>BamHI</td><td>11582, 6674</td></tr>
-<tr><td>AsLOVpep; pUPD2 </td><td>NotI</td><td>2558, 512</td></tr>
-</div></table>
-<p>Make an agarose gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31 (C4)</td><td>phyC31 (C5)</td><td>AsLOVpep (C4)</td><td>LexA:PIF:phy:ren+opLex:luc (C1)</td></tr>
-<tr><td>no</td><td>no</td><td>No</td><td>No</td></tr>
-<tr><td>LexA:KNdronpa:ren+OpLex:Luc (C3)</td><td>Gal4:KNdronpa:ren+UAS:luc (C1)</td><td>Gal4:KNdronpa:ren+UAS:luc
-(C2)</td><td>Gal4:KNdronpa:ren+UAS:luc (C3)</td></tr>
-<tr><td>Ok</td><td>no</td><td>no</td><td>No</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren</td><td>Reporter phiC31 (C1)</td><td></td></tr>
-<tr><td>no</td><td>Ok</td><td></td></tr>
-</div></table>
-<p>Only LexA:KNdronpa:ren+OpLex:Luc and Reporter phiC31 were correct. Repeat the ligations because is the second digestion
-of this construction that were made.</p>
-<ul><li>Measurement of DNA concentration:</li>
-<ul class="ul_2"><li>Reporter:phyC31: 13.6 ng/µl</li>
-<li>PhyC31: 4.6 ng/µl </li>
-<li>AsLOVpep: 30.3 ng/µl</li>
-<li>Igem151 (op:LexAluc): 40 ng/µl</li>
-<li>Gal4:PIF:phyB:ren (C1): 124.4 ng/µl</li>
-<li>LacI:PIF:phyB:VP16 (C1): 126 ng/µl</li>
-<li>Igem 159 (renilla): 42 ng/µl</li>
-<li>Gal4:Kdronpa:Ndronpa:renilla (C3): 172.8 ng/µl</li>
-<li>Igem 227 (op:UAS:luc): 6.3 ng/µl</li>
-</ul></ul>
-<ul><li>Pick colonies and make liquid culture of LacI:KDronpa:NDronpa:ren:luc (C4 and C5). The colonies of
-Gal4:PIF:phy:VP16+ren were all blue.</li>
-</ul>
-</br><h3 style="color:green">15 July 2015</h3>
-<ul><li>Miniprep of LacI:KDronpa:NDronpa:ren:luc (C4 and C5). </li>
-<li>Digestion:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:KDronpa:NDronpa:ren:luc</td><td>EcoRI</td><td>6345, 9965</td></tr>
-</div></table>
-<ul><li>Make the gel:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:K:NDronpa:ren:luc C4</td><td>LacI:K:NDronpa:ren:luc C5</td></tr>
-<tr><td>no</td><td>no</td></tr>
-</div></table>
-<ul><li>Measurement of DNA concentrations:</li>
-<ul class="ul_2"><li>Gal4BD:PIF:PhyB:VP16: 125.6 ng/µl</li>
-<li>LexA:PIF:phyB:VP16:ren: 322.6 ng/µl</li>
-<li>LacI:Kdronpa:NDronpa:ran: 209.0 ng/µl</li>
-</ul></ul>
-<ul><li>We decided to repeat the ligations due to that we make twice the digestions and we didn’t obtain good results.
-</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2</td><td>AsLOVpep; pUPD2</td><td>LacI:PIF:Phy:VP16+ren; a1</td></tr>
-<tr><td>1 µl phiC31</td><td>1 µl AsLOVpep</td><td>1.5 µl LacI:PIF:Phy:VP16</td></tr>
-<tr><td>1 pUPD2</td><td>1 pUPD2</td><td>2.5 µl renilla (159)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td><td>1 µl BSAI</td></tr>
-<tr><td>5.6 µl H2O</td><td>5.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td></td><td>0.5 µl a1</td></tr>
-<tr><td>Gal4:PIF:phy:VP16+ren; a1</td><td>LexA:PIF:phy:ren+opLex:luc; ?1</td><td>LacI:KNdronpa:ren+OpLex:Luc; ?1</td></tr>
-<tr><td>1.5 µl Gal4:PIF:phy:VP16</td><td>1 µl LexA:PIF:phy:ren</td><td>1 µl LacI:KNdronpa:ren</td></tr>
-<tr><td>2 µl renilla (159)</td><td>2.5 µl opLex:luc (151)</td><td>3 µl OpLac:Luc (152)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA </td><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BSAI</td><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>2.6 µl H2O</td><td>2.6 µl H2O</td><td>3 µl H2O</td></tr>
-<tr><td>1 µl a1</td><td>0.5 µl ?1</td><td>0.5 µl ?1</td></tr>
-<tr><td>Gal4:KNdronpa:ren+OpLex:Luc; ?1</td><td>PhyB:VP16+PIF6; ?1</td></tr>
-<tr><td>1 µl Gal4:KNdronpa:ren</td><td>1 µl PhyB:VP16 (88E)</td></tr>
-<tr><td>4 µl OpUAS:Luc (227)</td><td>2 µl PIF6 (170)</td></tr>
-<tr><td>1.2 µl buffer</td><td>1.2 µl buffer</td></tr>
-<tr><td>1.2 µl BSA</td><td>1.2 µl BSA</td></tr>
-<tr><td>1 µl T4 ligase</td><td>1 µl T4 ligase</td></tr>
-<tr><td>1 µl BsmbI</td><td>1 µl BsmbI</td></tr>
-<tr><td>3 µl H2O</td><td>3.6 µl H2O</td></tr>
-<tr><td>0.5 µl ?1</td><td>1 µl ?1</td></tr>
-</div></table>
-<ul><li>These <i>Agrobacterium</i> cultures have been refreshed:</li>
-<ul class="ul_2"><li>PIF-phyB-luc</li>
-<li>Renilla</li>
-<li>Pnos</li>
-<li>Etr8</li>
-</ul></ul>
-</br><h3 style="color:green">16 July 2015</h3>
-<ul><li>Yesterday ligations have been transformed into <i>E. coli</i>:</li>
-<ul class="ul_2"><li>phyC31;pUPD2</li>
-<li>AsLOVpep; pUPD2</li>
-<li>LacI:PIF:Phy:VP16+ren; a1</li>
-<li>Gal4:PIF:phy:VP16+ren; a1</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1</li>
-<li>LacI:KNdronpa:ren+OpLex:Luc; ?1</li>
-<li>Gal4:KNdronpa:ren+OpLex:Luc; ?1</li>
-<li>PhyB:VP16+PIF6; ?1</li>
-</ul></ul>
-<ul><li>The agroinfiltrated leaf with BxbI:rep:GFP has been observed in the magnifying glass with fluorescent lights. The
-efficiency of the recombinase is lower and it can not been observed a lot of green spots. Tomorrow another leaf will be
-seen to check again the construction.</li>
-</ul>
-<ul><li>Second refresh of the <i>Agrobacterium</i> cultures:</li>
-<ul class="ul_2"><li>PIF-phyB-luc</li>
-<li>Renilla</li>
-<li>Pnos</li>
-<li>Etr8</li>
-</ul></ul>
-<ul><li>Miniprep of these cultures.</li>
-<li>Digestion of the minipreps:</li>
-</ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PIF-phyB-luc; ?1</td><td>EcoRI</td><td>??</td></tr>
-<tr><td>Renilla; ?2</td><td>HindIII</td><td>No lo encuentro</td></tr>
-<tr><td>Pnos; ?1</td><td>EcoRI</td><td>2997, 353</td></tr>
-<tr><td>Etr8; ?1</td><td>EcoRI</td><td></td></tr>
-</div></table>
-<p>The digestions had positive controls that were included in the gel to compare the results obtained.</p>
-<p>The digestions are left overnight in the working table.</p>
-</br><h3 style="color:green">17 July 2015</h3>
-<p>Do the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>No se lo que pone?</td><td></td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-</div></table>
-<ul><li>Liquid culture of the colonies in the agar plates have been made, 3 colonies for each construction.</li>
-<li>OD’s mesurement for the agroinfiltration.</li>
-<ul class="ul_2"><li>Dilution 1:10 in MES.</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-</br><h3 style="color:green"> </h3>
-<tr><td>PIF:phyB:luc</td><td>0.47</td><td>41 µl/ml</td><td>630 µl</td></tr>
-<tr><td>Renilla</td><td>0.28</td><td>71 µl/ml</td><td>1065 µl</td></tr>
-<tr><td>Etr8:luc</td><td>0.32</td><td>52 µl/ml</td><td>930 µl</td></tr>
-<tr><td>Pnos</td><td>0.34</td><td>59 µl/ml</td><td>885 µl</td></tr>
-</div></table>
-<ul><li>Red toggle experiement:</li>
-</ul>
-<p>The plants were coinfiltrated with the red toggle (PIF+phyB) and renilla. Also with two controls, Pnos (positive
-control) and Etr8 (negative control).</p>
-<p>14 plants were used with 3 infiltrated leafs for each plants and two spots per leaf.</p>
-<p>The controls have been infiltrated in leafs of the plants like is shown in the picture. Pnos in the right part and Etr8
-in the left part.</p>
 <p> </p>
+				    </div>
+				</details>
+			</div>
-<p>Two plants were infiltrated with both controls in the three leafs and they were in natural light during all the
+				<br/>
+<ul class="actions" style="text-align:right">
-experiment. </p>
+<li><a href="https://2015.igem.org/Team:Valencia_UPV/Notebook/Content#scroll1" class="button alt">Go to Daily notebook</a></li>
-<p>Another 4 plants were infiltrated with controls following the same pattern in the procedure. </p>
-<p>The remaining 8 plants were infiltrated with the red toggle.</p>
-<p>Immediately after the infiltration the plants were distributed in three different conditions: natural light, darkness
-and far red.</p>
-<p>So after the agroinfiltration 2 control plants stay in natural light all the experiment; 2 control plants and 4 red
-toggle went into the far red chamber and the same amount of control and red toggle plan (2+4) went put in darkness.</p>
-<p>This conditions were maintained 3 days and then all the infiltrated leafs were cut into small discs and put into a
-special plates with water. </p>
-<p>In this moment was set the time 0 (21/07/2015 at 19:30) and take the first samples.</p>
-<p>Then in time 0 some of the dark and far red samples were put in red conditions to activate the red toggle.</p>
-<p>This scheme represent the distribution of samples and the times that were taken the samples.</p>
-<p>Hacer el esquema!!! Cuando este mas espabilada ;)</p>
-<p>It was observed another leaf with the recombinase BxbI with GFP in the magnifying glass with fluorescent lights. It was
-not observed a lot of spots, the efficiency is very low.</p>
-</br><h3 style="color:green">18 July 2015</h3>
-<p>23 minipreps of the liquid cultrures. LexA:PIF:phtB:ren:luc (C3) has not grown.</p>
-<p>Digestions of the minipreps:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2</td><td>NotI</td><td>2046, 1899</td></tr>
-<tr><td>AsLOVpep; pUPD2</td><td>NotI</td><td></td></tr>
-<tr><td>2046, 521</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren; a1</td><td>EcoRI</td><td>6345, 5623, 5487</td></tr>
-<tr><td>Gal4:PIF:phy:VP16+ren; a1</td><td>EcoRI</td><td>6345, 5487, 4852</td></tr>
-<tr><td>LexA:PIF:phy:ren+opLex:luc; ?1</td><td>BamHI</td><td>9431, 6674, 3513</td></tr>
-<tr><td>LacI:KNdronpa:ren+OpLex:Luc; ?1</td><td>BamHI</td><td>12632, 6574</td></tr>
-<tr><td>Gal4:KNdronpa:ren+OpLex:Luc; ?1</td><td>BamHI</td><td>11582, 6674</td></tr>
-<tr><td>PhyB:VP16+PIF6; ?1</td><td>BamHI</td><td>6674, 2685, 2337, 1439</td></tr>
-</div></table>
-<p>Gel has been done:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31 C1</td><td>phyC31 C2</td><td>phyC31 C3</td><td>AsLOVpep C1</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>ok</td></tr>
-<tr><td>AsLOVpep C2</td><td>AsLOVpep C3</td><td>Gal4:PIF:phy:VP16:ren C1</td><td>Gal4:PIF:phy:VP16:ren C2</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>no</td></tr>
-<tr><td>Gal4:PIF:phy:VP16:ren C3</td><td>LacI:PIF:phy:ren C1</td><td>LacI:PIF:phy:ren C2</td><td>LacI:PIF:phy:ren
-C3</td></tr>
-<tr><td>no</td><td>ok</td><td>no</td><td>No</td></tr>
-<tr><td>LexA:PIF:phy:ren:luc C1</td><td>LexA:PIF:phy:ren:luc C2</td><td>Gal4:KNdronpa:ren:luc
-C1</td><td>Gal4:KNdronpa:ren:luc C2</td></tr>
-<tr><td>no</td><td>no</td><td>ok</td><td>No</td></tr>
-<tr><td>Gal4:KNdronpa:ren:luc C3</td><td>LacI:KNdronpa:ren:luc C1</td><td>LacI:KNdronpa:ren:luc
-C2</td><td>LacI:KNdronpa:ren:luc C3</td></tr>
-<tr><td>no</td><td>no</td><td>ok</td><td>No</td></tr>
-<tr><td>PhyB:VP16:PIF6 C1</td><td>PhyB:VP16:PIF6 C2</td><td>PhyB:VP16:PIF6 C3</td><td></td></tr>
-<tr><td>ok</td><td>no</td><td>no</td><td></td></tr>
-</div></table>
-<p>Pick more colonies of:</p>
-<ul><li>Gal4:PIF:phy:VP16+ren; a1</li>
-<li>LexA:PIF:phy:ren+opLex:luc; ?1</li>
-</ul></ul>
-<p>New digestions with new enzymes:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>phyC31;pUPD2</td><td>XhoI (buffer red)</td><td>2119, 934, 894</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren; a1</td><td>NEB4</td><td>5949, 5653, 3610, 2246</td></tr>
-<tr><td>LacI:PIF:Phy:VP16+ren; a1</td><td>HindIII</td><td>11568, 5587</td></tr>
-</div></table>
-<p>After 3 digestions of LacI:PIF:Phy:VP16+ren; a1 is accepted the construction.</p>
-<p>It was observed another leaf with the recombinase BxbI with GFP in the magnifying glass with fluorescent lights. It was
-not observed a lot of spots, the efficiency is very low. This is the 4th day…</p>
-</br><h3 style="color:green">19 July 2015</h3>
-</br><h3 style="color:green">20 July 2015</h3>
-</br><h3 style="color:green">21 July 2015</h3>
-<ul><li>Red toggle experiment:</li>
 </ul>
-<p>Time lapses: </p>
+			</section>
-<p>-19:00=t0</p>
-<p>-1:00=t1</p>
-<p>-7:00= t2</p>
-<p>-19:00= t3 (it was taken the controls in natural light)</p>
-<ul><li>Minipreps of the colonies that were in 37ºC.</li>
-<ul class="ul_2"><li>LexA:PIF:Phy:ren:luc (C1 and C2)</li>
-<li>PhyC31 (C1, C2, C4 and C5)</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:PIF:Phy:ren:luc</td><td>BamHI</td><td>9431, 6674, 3513</td></tr>
-<tr><td>PhyC31</td><td>NotI</td><td>2046, 1899</td></tr>
-</div></table>
-<p>Gel with the digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PhyC31 C1</td><td>PhyC31 C2</td><td>PhyC31 C4</td><td>PhyC31 C5</td></tr>
-<tr><td>Ok?</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>LexA:PIF:Phy:ren:luc C1</td><td>LexA:PIF:Phy:ren:luc C2</td><td></td></tr>
-<tr><td>No DNA</td><td>No DNA</td><td></td></tr>
-</div></table>
-<p>We had problems with some colonies because in the digestion did not appear DNA. The minipreps will be made with a
-better kit.</p>
-<p>Transform in <i>Agrobacterium</i> this cultures:</p>
-<ul><li>LexABD:KDronpa:NDronpa:ren:luc</li>
-<li>Gal4BD:KDronpa:NDronpa:ren:luc</li>
-<li>LacIBD:KDronpa:NDronpa:ren:luc</li>
-<li>OpLexA:luc (151)</li>
-<li>OpUAS:luc</li>
-<li>OpLacI:luc (152)</li>
-</ul></ul>
-<p>It was made liquid culture of Gal4:PIF:phyB:ren; ?1 (C1-C5)</p>
-<p>It was made ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>35S:Gal4:AsLOVpep:T35S; ?1</td><td>35S:LacI:AsLOVpep:T35S; ?1</td><td>35S:LexA:AsLOVpep:T35S; ?1</td></tr>
-<tr><td>1 µl 35S (0030)</td><td>1 µl 35S (0030)</td><td>1 µl 35S (0030)</td></tr>
-<tr><td>1 µl Gal4BD</td><td>1 µl LacI</td><td>1 µl LexA</td></tr>
-<tr><td>1 µl AsLOVpep </td><td>1 µl AsLOVpep </td><td>1 µl AsLOVpep </td></tr>
-<tr><td>1 µl T35S (0036)</td><td>1 µl T35S (0036)</td><td>1 µl T35S (0036)</td></tr>
-<tr><td>1 µl ?1 </td><td>1 µl ?1 </td><td>1 µl ?1 </td></tr>
-<tr><td>2.6 µl H2O</td><td>2.6 µl H2O</td><td>2.6 µl H2O</td></tr>
-<tr><td>PsinATG:RepPhiC31:GFP:T35S; ?2</td><td>LacI:PIF:PhyB:ren+luc; ?1</td><td>PIF:PhyB+renilla; ?2</td></tr>
-<tr><td>1 µl PsinATG (552)</td><td>1.5 µl LacI:PIF:PhyB:ren; ?1</td><td>1.5 µl PIF:PhyB</td></tr>
-<tr><td>1 µl ReporterPhyC31</td><td>3 µl OpLacI:luc (152); ?2</td><td>2.5 µl renilla (159)</td></tr>
-<tr><td>1 µl GFP (0059)</td><td>0.5 µl ?1</td><td>0.5 µl ?2</td></tr>
-<tr><td>1 µl T35S (0036)</td><td>2.6 H2O</td><td>3 µl H2O</td></tr>
-<tr><td>1 µl ?2 </td><td></td></tr>
-<tr><td>2.6 µl H2O</td><td></td></tr>
-</div></table>
-<p>Luciferase essay with all the samples collected in the last three days.</p>
-<ul><li>Sampling: 25 samples in total.</li>
-<li>Passive lysis 1x (200µl/sample x 25 samples)= 5.000 µl</li>
-<li>Crush samples.</li>
-<li>Add 150 µl of passive lysis buffer and mix in the vortex.</li>
-<li>Centrifuge at 13200rpm for 15’.</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>E8/li</td><td>E8/li</td><td>E8/li</td><td>P/li</td><td>P/li</td><td>P/li</td><td>TR/Fr</td><td>TR/Fr</td><td>TR/Fr
-</td><td>TR/D</td><td>TR/D</td><td>TR/D</td></tr>
-<tr><td>TR/Fr</td></tr>
-<tr><td>Red</td><td>TR/Fr</td></tr>
-<tr><td>Red</td><td>TR/r</td></tr>
-<tr><td>Red</td><td>TR/D</td></tr>
-<tr><td>Red</td><td>TR/D</td></tr>
-<tr><td>Red</td><td>TR/D</td></tr>
-<tr><td>Red</td><td></td><td></td><td></td></tr>
-</div></table>
-<p>We used 14.4 µl of Stop and Glow. 705.6 destilled H2O</p>
-</br><h3 style="color:green">22 July 2015</h3>
-<p>Miniprep of Gal4:PIF:PhyB:ren (C1-C3) C4 and C5 did not grow.</p>
-<p>Digestion of the miniprep:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4:PIF:PhyB:ren</td><td>BamHI</td><td>16684</td></tr>
-<tr><td></td><td>EcoRI</td><td>4852, 5487, 6345</td></tr>
-<tr><td></td><td>EcoRV</td><td>1849, 3942, 2475, 381, 8037</td></tr>
-</div></table>
-<p>Gel was made:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4… (BamHI)</td><td>Gal4… (EcoRI)</td><td>Gal4… (EcoRV)</td></tr>
-<tr><td>no</td><td>no</td><td>no</td></tr>
-</div></table>
-<p>After doing several digestions with different enzyme all with wrong band patterns, it was decided to revise each part
-making digestions. The parts are: </p>
-<ul><li>PhyC31; pUPD2</li>
-<li>Gal4:PIF:phyB; </li>
-<li>Renilla (GB159)</li>
-</ul></ul>
-<p>Made liquid culture of the ReporterBxbI:GFP in <i>Agrobacterium</i>.</p>
-<p>Transform the ligations into <i>E. coli</i>:</p>
-<ul><li>35S:Gal4:AsLOVpep:T35S; ?1</li>
-<li>35S:LacI:AsLOVpep:T35S; ?1</li>
-<li>35S:LexA:AsLOVpep:T35S; ?1</li>
-<li>PsinATG:RepPhiC31:GFP:T35S; ?2</li>
-<li>LexA:PIF:PhyB:ren+luc; ?1</li>
-<li>Add 300 µl of SOC medium and put into a agar plate with the corresponding antibiotics.</li>
-</ul></ul>
-<p>Luciferase essay:</p>
-<ul><li>Sampling: samples that have been in red and natural light 48h, 3 samples.</li>
-<li>200 µl/sample x 3 sample= 600 µl of passive lissis buffer (5x)</li>
-<li>Passive lissis buffer 1x= 120 µl+480 µl water.</li>
-<li>2.4 µl of Stop and glow</li>
-<li>118 µl of  buffer.</li>
-</ul></ul>
-</br><h3 style="color:green">23 July 2015</h3>
-<p>We decided to infiltrate soybean sprouts. First we decided to infiltrate with dye to observe the characteristics and
-the capacity of absorption.</p>
-<p> </p>
-<p>Mesurement of the ODs to agroinfiltrate:</p>
-<p>The samples are:</p>
-<ul><li>Citoplasm=0.27</li>
-<li>DsRed=0.27</li>
-<li>GFP=0.36</li>
-<li>Recombinase=0.43</li>
-</ul></ul>
-<p>Vi= (Vf*Absf)/(Absi*10)</p>
-<p>Absi=0.1 (because is a viral system)</p>
-<p>Vf=120 µl</p>
-<p>Make 16 liquid culture of the white colonies in the agar plates.</p>
-</br><h3 style="color:green">24 July 2015</h3>
-<p>Minipreps of the 13 liquid culture. LacI:PIF:phyB:ren cultures did not grow.</p>
-<p>Digestion of the minipreps:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4:AsLOVpep</td><td>EcoRI</td><td>6345, 1972</td></tr>
-<tr><td>LacI:AsLOVpep</td><td>EcoRI</td><td>6345, 2743</td></tr>
-<tr><td>LexA:AsLOVpep</td><td>EcoRI</td><td>6345, 2011</td></tr>
-<tr><td>PsinATG:RepPhiC31:GFP</td><td>HindIII</td><td>6345, 2691</td></tr>
-<tr><td>LexA:PIF:PhyB:ren+luc</td><td>BamHI</td><td>9431, 6674, 3513</td></tr>
-<tr><td></td><td></td></tr>
-<tr><td>PhyC31; pUPD2</td><td>NotI</td><td>2046, 1899</td></tr>
-<tr><td>Gal4:PIF:phyB</td><td>BamHI</td><td>6674, 3474, 2337</td></tr>
-<tr><td>Renilla (GB159)</td><td>EcoRV</td><td>2909, 2475, 882, 812, 381</td></tr>
-</div></table>
-<p>It was done 2 gels with ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4:AsLOV C1</td><td>Gal4:AsLOV C2</td><td>Gal4:AsLOV C3</td><td>PsinATG:RepPhi</td></tr>
-<tr><td>C31:GFP C1</td><td>PsinATG:RepPhi</td></tr>
-<tr><td>C31:GFP C2</td><td>PsinATG:RepPhi</td></tr>
-<tr><td>C31:GFP C3</td></tr>
-<tr><td>ok</td><td>ok</td><td>ok</td><td>ok</td><td>no</td><td>No</td></tr>
-<tr><td>Mw/ladder</td><td>LacI:AsLOV C1</td><td>LacI:AsLOV C2</td><td>LexA:AsLOV C1</td><td>LexA:AsLOV
-C2</td><td>LexA:AsLOV C3</td></tr>
-<tr><td>-</td><td>ok</td><td>No</td><td>no</td><td>ok</td><td>no</td></tr>
-<tr><td>LexA:PIF:PhyB:ren+luc C1</td><td>LexA:PIF:PhyB:ren+luc C2</td><td></td><td></td></tr>
-<tr><td>no</td><td>Ok</td><td></td><td></td></tr>
-</div></table>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PhyC31 (C1)</td><td>PhyC31 (C2)</td><td>PhyC31 (C3)</td><td>PhyC31 (C4)</td><td>PhyC31 (C5)</td></tr>
-<tr><td>no</td><td>ok</td><td>ok</td><td>ok</td><td>no</td></tr>
-<tr><td>Gal4:PIF:phyB</td><td>Renilla (GB159)</td><td></td><td></td></tr>
-<tr><td>ok</td><td>Ok</td><td></td><td></td></tr>
-</div></table>
-</br><h3 style="color:green">26 July 2015</h3>
-<p>Liquid cultures of <i>Agrobacterium</i> were refreshed:</p>
-<ul><li>TsinATG:BxbIreporter:GFP</li>
-<li>TsinATG:BxbI:reporterBxbI:GFP</li>
-<li>Viral vector??no se cual es</li>
-</ul></ul>
-</br><h3 style="color:green">27 July 2015</h3>
-<p>Sent to sequence:</p>
-<ul><li>210.08.256: LacIBD; pUPD2 (C1)</li>
-<li>210.08258: Gal4BD; pUPD2 (C2)</li>
-<li>210.08.259:LexABD; pUPD2 (C1) </li>
-<li>210.08.260: PIF6; pUPD2 (C5)</li>
-<li>210.08.261: VP16; pUPD2 (C1)</li>
-<li>210.08.262: PhiC31; pUPD2 (C2)</li>
-<li>210.08.264: PhiC31; pUPD2 (C3)</li>
-<li>210.08.266: PhiC31; pUPD2 (C4)</li>
-<li>210.08.268: ReporterBxbI; pUPD2 (C1)</li>
-<li>210.08.269: ReporterPhiC31; pUPD2 (C1)</li>
-<li>210.08.270: AsLOVpep; pUPD2 (C1)</li>
-</ul></ul>
-<p>The sample had to have 10µl of miniprep (200ng/µl aprox) + 5 µl of primer (dilution 1:3)</p>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Gal4:PIF:phiB + ren; ?1</td><td>LacI:PIF:phiB:ren + luc; ?2</td><td>PIF:PhyB+renilla; ?2</td></tr>
-<tr><td>1.5 µl Gal4:PIF:phiB</td><td>1.5 µl LacI:PIF:phiB:ren</td><td>1.5 µl PIF:phiB</td></tr>
-<tr><td>2 µl Renilla (GB159)</td><td>2 µl OpLacI:luc</td><td>2.5 µl Renilla (GB159)</td></tr>
-<tr><td>0.5 µl ?1</td><td>0.5 µl ?2</td><td>0.5 µl ?2</td></tr>
-<tr><td>3.6 µl H2O</td><td>2.6 µl H2O</td><td>3 µl H2O</td></tr>
-</div></table>
-<p>OD’s measurements to prepare the agroinfiltrates:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Cytoplasm: 0.39 (viral)</td><td>0.25ml</td></tr>
-<tr><td>Integrase: 0.35 (viral)</td><td>0.28ml</td></tr>
-<tr><td>GFP: 0.32 (viral)</td><td>0.31ml</td></tr>
-<tr><td>Dsred: 0.31 (viral)</td><td>0.32ml</td></tr>
-<tr><td>BxbI:reporter: 0.41</td><td>0.49ml</td></tr>
-<tr><td>Reporter: 0.26</td><td>0.77ml</td></tr>
-</div></table>
-<p>3 plants were infiltrated with BxbI and the reporter of BxbI (one leaf with the control an the other with the
-recombinase)?? No entiendo lo de la libreta </p>
-<p>Ligations to join the negative controls with renilla:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Etr8:luc+staffer (SF)</td><td>OpLexA:luc+SF</td><td>OpLacI:luc+SF</td><td>UAS:luc+SF</td></tr>
-<tr><td>1.5 µl Etr8:luc (88C o 1098)</td><td>1.5 µl OpLexA:luc (151)</td><td>1.5 µl OpLacI:luc (152)</td><td>1.5 µl
-UAS:luc (227)</td></tr>
-<tr><td>1 µl SF; ?2</td><td>1 µl SF; ?2</td><td>1 µl SF; ?2</td><td>1 µl SF; ?2</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>6.1 µl H2O</td><td>6.1 µl H2O</td><td>6.1 µl H2O</td><td>6.1 µl H2O</td></tr>
-</div></table>
-<p>Transformation of <i>E. coli</i> of the ligations:</p>
-<ul><li>Gal4:PIF:phiB + ren; ?1</li>
-<li>LacI:PIF:phiB:ren + luc; ?2</li>
-<li>PIF:PhyB+renilla; ?2</li>
-</ul></ul>
-<p>Make cultures in agar petri dishes of the transformations with the corresponding antibiotics.</p>
-<p>Transformation into <i>Agrobacterium</i> with the constructions:</p>
-<ul><li>Gal4:KDronpa:NDronpa:ren:luc</li>
-<li>LacI:KDronpa:NDronpa:ren:luc</li>
-<li>LexA:KDronpa:NDronpa:ren:luc</li>
-<li>OpLexA:luc (GB 151)</li>
-<li>OpLacI:luc (GB 152)</li>
-<li>UAS:luc (GB 227)</li>
-</ul></ul>
-<p>Make cultures in agar petri dishes of the transformations with the corresponding antibiotics.</p>
-<p>It was received a new piece (ePDZ) which is part of the blue toggle (plan A). It arrived in E.coli so it was made a
-lquid culture and let it grow at 37ºC overnight.</p>
-</br><h3 style="color:green">28 July 2015</h3>
-<p>Miniprep of the liquid culture: ePDZ.</p>
-<p>Transformation into E.coli of the ligations:</p>
-<ul><li>Etr8:luc+staffer (SF)</li>
-<li>OpLexA:luc+SF</li>
-<li>OpLacI:luc+SF</li>
-<li>UAS:luc+SF</li>
-<li>Gal4:PIF:phyB:ren</li>
-</ul></ul>
-<p>It was observed the soybean sprouts that were infiltrated with a dye with green light and red filter. It was not
-observed nothing significant, moreover, the damage is evident. </p>
-<p>Transformation in <i>Agrobacterium</i> the ReporterPhiC31:GFP.</p>
-<p>Pick colonies and make liquid cultures adding X-Gal and IPTG because the colonies were little and we can not observe
-clearly if they were white or blue.</p>
-<ul><li>Gal4:PIF:phiB + ren. Did not grow any colony.</li>
-<li>LacI:PIF:phiB:ren + luc (C1-C3)</li>
-<li>PIF:PhyB+renilla (C1- C3)</li>
-</ul></ul>
-<p>The medicine LTB (heat labile toxin B subunit) which is part of an enterotoxin of Echerichia coli homologous to the
-same toxin in Vibrio cholerae that causes diarrhea. </p>
-<p>We add 50µl to have a final concentration of 10ng/µl.</p>
-<p>Ligation:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LTB; pUPD2</td></tr>
-<tr><td>1 µl LTB</td></tr>
-<tr><td>1 µl pUPD2</td></tr>
-<tr><td>5.6 µl H2O</td></tr>
-</div></table>
-</br><h3 style="color:green">29 July 2015</h3>
-<p>Miniprep of yesterday liquid culture:</p>
-<ul><li>LacI:PIF:phiB:ren + luc (C1 and C3) C2 turn into blue.</li>
-<li>PIF:PhyB+renilla (C2) C1 and C3 did not grow.</li>
-</ul></ul>
-<p>Digestion:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:PIF:phiB:ren:luc</td><td>EcoRV</td><td>882, 968, 1652, 3942, 2475, 381, 3477, 6674</td></tr>
-<tr><td>PIF:PhyB+renilla</td><td>HindIII</td><td>4316, 5887, 788, 6345</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:PIF:phiB:ren:luc (C1)</td><td>LacI:PIF:phiB:ren:luc (C3)</td><td>PIF:PhyB+renilla (C2)</td></tr>
-<tr><td>no</td><td>no</td><td>no</td></tr>
-</div></table>
-<p>Pick colonies and make liquid culture of:</p>
-<ul><li>Etr8:luc:staffer(SF) (C1-C3)</li>
-<li>OpLexA:luc:SF (C1-C3)</li>
-<li>OpLacI:luc:SF (C1-C3)</li>
-<li>UAS:luc:SF (C1-C3)</li>
-<li>Gal4:PIF:phyB:ren (C1-C3)</li>
-</ul></ul>
-<p>Transformation in E.coli of:</p>
-<ul><li>LTB; pUPD2</li>
-</ul></ul>
-</br><h3 style="color:green">30 July 2015</h3>
-<p>Minipreps have been done:</p>
-<ul><li>Etr8:luc:staffer(SF) (C1-C3)</li>
-<li>OpLexA:luc:SF (C1 and C3) C2 did not grow.	</li>
-<li>OpLacI:luc:SF (C1-C3)</li>
-<li>UAS:luc:SF (C1-C3)</li>
-<li>Gal4:PIF:phyB:ren (C1-C3)</li>
-</ul></ul>
-<ul><li>LacI:PIF:phy:ren:luc (C1-C3)</li>
-<li>PIF:phyB:ren (C1-C3)</li>
-</ul></ul>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Etr8:luc:staffer(SF)</td><td>BamHI</td><td>6674, 2766</td></tr>
-<tr><td>OpLexA:luc:SF</td><td>BamHI</td><td>6674, 2746</td></tr>
-<tr><td>OpLacI:luc:SF</td><td>BamHI</td><td>6674, 2847</td></tr>
-<tr><td>UAS:luc:SF</td><td>BamHI</td><td>6674, 2568</td></tr>
-<tr><td>Gal4:PIF:phyB:ren</td><td>EcoRI</td><td>6345, 5487, 4852</td></tr>
-<tr><td>LacI:PIF:phy:ren:luc</td><td>BamHI</td><td>20451</td></tr>
-<tr><td>PIF:phyB:ren</td><td>HindIII</td><td>6345, 5887, 4316, 788</td></tr>
-</div></table>
-<p>Do the gel:</p>
-<p>No se el orden!! Preguntar </p>
-<p>Primers have arrived:</p>
-<ul><li>ePDZ reverse and forward and phyC31.</li>
-</ul></ul>
-<p>Make a PCR with ePDZ and its primers to obtain the desired fragment and put it in pUPD2.</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>ePDZ PCR</td></tr>
-<tr><td>10µl Buffer HF</td></tr>
-<tr><td>31.5 µl H2O</td></tr>
-<tr><td>2 µl dNTPs</td></tr>
-<tr><td>2.5 µl  Primer forward</td></tr>
-<tr><td>2.5 µl primer reverse</td></tr>
-<tr><td>1 µl ePDZ (dilution 1:50)</td></tr>
-<tr><td>0.5 µl Taq phunion</td></tr>
-</div></table>
-<p>Pick 2 colonies of phiC31:GFP in <i>Agrobacterium</i> and make liquid culture.</p>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>ePDZ; pUPD2</td><td>PIF:phyB+ren; ?2</td><td>OpUAS:luc:SF+ren; ?1</td><td>OpLexA:luc:SF+ren; ?1</td></tr>
-<tr><td>1 µl ePDZ</td><td>1 µl PIF:phyB</td><td>1 µl OpUAS:luc:SF</td><td>1 µl OpLexA:luc:SF</td></tr>
-<tr><td>1 µl pUPD2</td><td>1 µl ren (159)</td><td>1 µl ren</td><td>1 µl ren</td></tr>
-<tr><td>5.6 µl H2O</td><td>1 µl ?2</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td></td><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-<tr><td>OpEtr8:luc:SF+ren; ?1</td><td>Op:LacI:luc:SF+ren; ?1</td></tr>
-<tr><td>1 µl OpEtr8:luc:SF</td><td>1 µl OpLacI:luc:SF</td></tr>
-<tr><td>1 µl ren</td><td>1 µl ren</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-<p>After 3 days till the agroinfiltration we have observed the leaf discs that have BxbI+repBxbI and the repBxbI (negative
-control). </p>
-<p>We could see that the level of GFP expression was higer in the infiltration with the recombinase but there was also
-expression in the negative control. We think that this can be a contamination due to that we had infiltrated both
-constructions in he same leaf and we did not change the gloves between agroinfiltrations. FOTOO!</p>
-<p>Make liquid culture (E.coli) of:</p>
-<ul><li>LTB; pUPD2 (C1-C3)</li>
-</ul></ul>
-</br><h3 style="color:green">31 July 2015</h3>
-<p>Ligation:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LacI:PIF:phyB:ren+OpLacI:luc; ?2</td></tr>
-<tr><td>1.5 µl LacI:PIF:phyB:ren</td></tr>
-<tr><td>3 µl OpLacI:luc</td></tr>
-<tr><td>0.5 µl ?2</td></tr>
-<tr><td>2.6 µl H2O</td></tr>
-</div></table>
-<p>After 4 days till the agroinfiltration we have observed again the samples with BxbI and the negative control but was
-the same. The negative control expressed GFP but less than the recombinase. Foto!</p>
-<p>Minipreps of liquid culture LTB (C1 and C2)</p>
-<p>Digestion:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LTB; pUPD2</td><td>NotI</td><td>2046, 474</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LTB (C1)</td><td>LTB (C2)</td><td>PCR ePDZ</td></tr>
-<tr><td>??</td><td></td></tr>
-</div></table>
-<p>Take out glicerynates of Paloma, lab mate:</p>
-<ul><li>Sip rotavirus CH2</li>
-<li>Sip rotavirus CH2-CH3</li>
-</ul></ul>
-<p>For E.coli and <i>Agrobacterium</i>.</p>
-<p>Pick a colony of Asun interferon (IFN) in Agro, make liquid culture.</p>
-<p>We had miniprep of IFN in pUPD. Make ligations.</p>
-<p>Transform in E.coli the ligations and make petri dishes cultures:</p>
-<ul><li>ePDZ; pUPD2</li>
-<li>PIF:phyB+ren; ?2</li>
-<li>OpUAS:luc:SF+ren; ?1</li>
-<li>OpLexA:luc:SF+ren; ?1</li>
-<li>OpEtr8:luc:SF+ren; ?1</li>
-<li>Op:LacI:luc:SF+ren; ?1</li>
-<li>LacI:PIF:phyB:ren+OpLacI:luc; ?2</li>
-</ul></ul>
-<p>Refresh agro cultures to agroinfiltrate tomorrow:</p>
-<ul><li>PhiC31 (viral system)</li>
-<li>ReporterPhiC31</li>
-<li>BxbI+reporterBxbI</li>
-<li>ReporterBxbI</li>
-<li>Gal4:KDronpa:NDronpa:luc:ren (brue toggle)</li>
-<li>PIF:phi:luc</li>
-<li>Renilla</li>
-<li>P19</li>
-<li>Pnos</li>
-</ul></ul>
-<p>New experiment with Nicotiana bentamiana. PROTOCOL</p>
-<p>Next constructions were agroinfiltrated, 2 or 3 leafs for each plant:</p>
-<p>PhiC31: one leaf for PhiC31+RepPhiC31+P19 (coinfiltration) and the other with RepPhiC31+P19 which is the negative
-control. 2 plants were infiltrated.</p>
-<p>BxbI: one leaf with BxbI:RepBxbI+P19 and the other with RepBxbI+P19 which is negative control. 2 plants were
-infiltrated.</p>
-<p>Red toggle: PIF6:phyB:luc+ren (coinfiltration). They were infiltrated 3 plants with 3 leafs for each.</p>
-<p>Blue toggle: Gal4:NDronpa:KDronpa:luc:ren. They were infiltrated 3 plants with 3 leafs for each.</p>
-<p>Pnos, the positive control. There are 4 plantas, 3 leafs per plant. </p>
-<p>So we will take samples in time 0, 12, 24 and 36h for each construction and control. After 2 days of the
-agroinfiltration (during this period all the plants were in dark, it is set time 0 we make discs os leaf and put in a
-plate with water and we change the conditions that were before. </p>
-<p>Red toggle plants: 9 discs stay in dark, 9 went to red and 9 went to natural light.</p>
-<p>Blue toggle: the same as red but went to ultraviolet instead of red light.</p>
-<p>Pnos: one plant were in natural light during all the experiment. The other discs will go, after the 2 days in black, to
-red, ultraviolet and stay in dark.</p>
-<p>Recombinases: they are in natural light during all the experiment.</p>
-</br><h3 style="color:green">1 August 2015</h3>
-<p>Prepare the <i>Agrobacterium</i> cultures for agroinfiltration:</p>
-<p>Gal4B:KDronpa:NDronpa:luc:ren, PhiC31 and its control, BxbI and its control and PIF:PhyB and its control were
-centrifugated 10 min at 3000g. The sobrenadant was discarded and the bacterias were resuspended with the agroinfiltration
-medium.</p>
-<p>Agroinfiltration medium had: 10ml MES, 1ml MgCl2, 89ml H2O, 100ml DMSO+acetosiningone.</p>
-<p>Incubate in 2h.</p>
-<p>Mesurement oof the ODs:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Ren+P19</td><td>0.09</td><td>888.9 µl</td></tr>
-<tr><td>RepPhiC31</td><td>0.69</td><td>115.94 µl</td></tr>
-<tr><td>BxbI</td><td>0.46</td><td>174 µl</td></tr>
-<tr><td>RepBxbI</td><td>0.15</td><td>533.3 µl</td></tr>
-<tr><td>Gal4:KNDronpa:ren:luc</td><td>0.51</td><td>156.9 µl</td></tr>
-<tr><td>Pnos</td><td>0.29</td><td>275.9 µl</td></tr>
-<tr><td>PIF:phy:luc</td><td>0.17</td><td>470.6 µl</td></tr>
-<tr><td>PhiC31</td><td>0.32</td><td>250 µl</td></tr>
-</div></table>
-<p>We went to the greenhouse and infiltrate the 13 plants.</p>
-<p>Look the petri dishes culture:</p>
-<ul><li>PIF:phyB+ren; ?2</li>
-<li>OpLexA:luc:SF+ren; ?1</li>
-<li>Op:LacI:luc:SF+ren; ?1</li>
-</ul></ul>
-<p>This colonies did not grow, the rest were left in the fridge.</p>
-<ul><li>ePDZ; pUPD2</li>
-<li>OpUAS:luc:SF+ren; ?1</li>
-<li>OpEtr8:luc:SF+ren; ?1</li>
-<li>LacI:PIF:phyB:ren+OpLacI:luc; ?2</li>
-</ul></ul>
-</br><h3 style="color:green">3 August 2015</h3>
-<p>Miniprep of the liquid culture:</p>
-<ul><li>Sip rotavirus CH2</li>
-<li>Sip rotavirus CH2-CH3</li>
-</ul></ul>
-<p>Measure of DNA concentration of:</p>
-<ul><li>OpLexA:luc:SF=169ng/µl</li>
-<li>OpacI:luc:SF=291ng/µl</li>
-</ul></ul>
-<p>Pick colonies gb159and make liquid culture of:</p>
-<ul><li>ePDZ; pUPD2 (C1-C3)</li>
-<li>OpUAS:luc:SF+ren; ?1(C1-C3)</li>
-<li>OpEtr8:luc:SF+ren; ?1(C1-C3)</li>
-<li>LacI:PIF:phyB:ren+OpLacI:luc; ?2 (C1-C3) Added X-gal and IPTG.</li>
-</ul></ul>
-<p>Repeat ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>OpLexA:luc:SF+ren; ?1</td><td>Op:LacI:luc:SF+ren; ?1</td><td>E-PIF:phyB+ren; ?2</td></tr>
-<tr><td>1 µl OpLexA:luc:SF</td><td>1 µl OpLacI:luc:SF</td><td>1 µl E-PIF:phy</td></tr>
-<tr><td>3 µl ren</td><td>3 µl ren</td><td>3 µl ren</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>2.6 µl H2O</td><td>2.6 µl H2O</td><td>2.6 µl H2O</td></tr>
-</div></table>
-<p>Refresh agrobacterium cultures of:</p>
-<ul><li>Interferon</li>
-<li>SIP-CH2</li>
-<li>SIP-CH2-CH3</li>
-</ul></ul>
-<p>Take the glycerinate of Renilla; ?2 (GB159) and make liquid culture.</p>
-<p>We have made all the leaf discs and put in order in the plates with 300 µl of water, also we put each plate in the
-conditions light that they have to be. We have taken the samples of time0 (13:00).</p>
-<p>So as T0= 13:00, T12=1:00, T24= 13:00 and T36= 1:00.</p>
-<p>Imagenes de la colocacion en los platos? Hace falta?</p>
-</br><h3 style="color:green">4 August 2015</h3>
-<p>We do a Western blot with Asun so we can learn how to do it. Lo copio? De verdad!!?</p>
-<p>Miniprep of the liquid cultures:</p>
-<ul><li>ePDZ; pUPD2 (C1-C3)</li>
-<li>OpUAS:luc:SF+ren; ?1(C1-C3)</li>
-<li>OpEtr8:luc:SF+ren; ?1(C1-C3)</li>
-<li>LacI:PIF:phyB+ren; ?2 (C2 and C3) C1 was blue.</li>
-</ul></ul>
-<p>Digestions:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>ePDZ; pUPD2</td><td>NotI</td><td>2046, 642</td></tr>
-<tr><td>OpUAS:luc:SF+ren; ?1</td><td>EcoRI</td><td>6345, 7096</td></tr>
-<tr><td>OpEtr8:luc:SF+ren; ?1</td><td>EcoRI</td><td>6345, 7294</td></tr>
-<tr><td>LacI:PIF:phyB:ren+OpLacI:luc; ?2</td><td>EcoRV</td><td>6674, 3477, 381, 2475, 3942, 1652, 968, 882</td></tr>
-<tr><td>Renilla 159</td><td>EcoRV</td><td>2909, 2475, 882, 812, 381</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>ePDZ C1</td><td>ePDZ C2</td><td>ePDZ C3</td><td>LacI:PIF:phyB+ren </td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td></td></tr>
-<tr><td>Renilla 159</td><td>OpUAS:luc:SF+ren C1</td><td>OpUAS:luc:SF+ren C2</td><td>OpUAS:luc:SF+ren C3</td></tr>
-<tr><td>Ok</td><td>¿?</td><td></td></tr>
-<tr><td>OpEtr8:luc:SF+ren C1</td><td>OpEtr8:luc:SF+ren C2</td><td>OpEtr8:luc:SF+ren C3</td><td></td></tr>
-<tr><td></td><td></td><td></td></tr>
-</div></table>
-<p>Transformation into E.coli of yesterday ligations:</p>
-<ul><li>OpLexA:luc:SF+ren; ?1</li>
-<li>Op:LacI:luc:SF+ren; ?1</li>
-<li>E-PIF:phyB+ren; ?2</li>
-</ul></ul>
-<p>Make petri dishes culture with the indicate antibiotic.</p>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>35S+ePDZ+VP16+T35S;?2</td><td>35S+LTB+T35S; ?1</td></tr>
-<tr><td>1µl ePDZ</td><td>1µl 35S (30)</td></tr>
-<tr><td>1 µl VP16</td><td>1µl T35S (36)</td></tr>
-<tr><td>1 µl 35S (30)</td><td>1µl LTB</td></tr>
-<tr><td>1 µl T35S (36)</td><td>1µl ?1</td></tr>
-<tr><td>1 µl ?2</td><td>3.6 µl H2O</td></tr>
-<tr><td>2.6 µl H2O</td><td></td></tr>
-</div></table>
-<p>Refresh agrobacterium cultures of:</p>
-<ul><li>Interferon</li>
-<li>SIP-CH2</li>
-<li>SIP-CH2-CH3</li>
-</ul></ul>
-</br><h3 style="color:green">5 August 2015</h3>
-<p>Transform ligations:</p>
-<ul><li>35S+ePDZ+VP16+T35S; ?2</li>
-<li>35S+LTB+T35S; ?1</li>
-</ul></ul>
-<p>Pick colonies and make liquid cultures cultures of:</p>
-<ul><li>OpLexA:luc:SF+ren; ?1 (C1-C3)</li>
-<li>Op:LacI:luc:SF+ren; ?1 (C1-C3)</li>
-<li>E-PIF:phyB+ren; ?2 (C1)</li>
-<ul class="ul_ul_ul_notebook"><li>35S+ePDZ+VP16+T35S; ?2 (C1 and C2)</li>
-</ul><li>35S+LTB+T35S; ?1 (C1 and C2)</li>
-</ul></ul>
-<p>Make luciferase essay of red and blue toggle:</p>
-<p>Number of samples=75 (a lot)</p>
-<p>1.	Prepare lisis buffer for 80 samples.</p>
-<p>200 µl/sample * 80sample = 16ml</p>
-<p>Buffer (5x)—3.2ml of buffer + 12.8ml H2O miliQ: lysis buffer (1x)</p>
-<p>2.	Crushed samples+ 150 µl of lysis buffer.</p>
-<p>3.	Centrifuge 15min at 13200rpm in cold.</p>
-<p>4.	Dilution 2:3 (Add 36 µl lysis buffer + 24 µl sample)</p>
-<p>5.	Luciferase: 40 µl/sample. Prepare 2.88ml (3 substrate tubes)</p>
-<p>6.	Renilla:….?</p>
-</br><h3 style="color:green">6 August 2015</h3>
-<p>Miniprep of the liquid cultures.</p>
-<p>Digestion:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>OpLexA:luc:SF+ren</td><td>EcoRI</td><td>6345, 7274</td></tr>
-<tr><td>Op:LacI:luc:SF+ren</td><td>EcoRI</td><td>6345, 7375</td></tr>
-<tr><td>E-PIF:phyB+ren</td><td>HindIII</td><td>6345, 788, 5887, 4316</td></tr>
-<tr><td>35S+ePDZ+VP16+T35S</td><td>HindIII</td><td>6345, 2316</td></tr>
-<tr><td>35S+LTB+T35S</td><td>EcoRI</td><td>6345, 1684</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PIF:phyB+ren</td><td>OpLexA:luc:SF+ren C1</td><td>OpLexA:luc:SF+ren C2</td><td>OpLexA:luc:SF+ren C3</td></tr>
-<tr><td>No</td><td>Ok, repeat</td><td>No</td><td>Ok, repeat</td></tr>
-<tr><td>Op:LacI:luc:SF+ren C1</td><td>Op:LacI:luc:SF+ren C2</td><td>Op:LacI:luc:SF+ren C3</td><td>35S+LTB+T35S
-C1</td></tr>
-<tr><td>Ok, repeat</td><td>Ok</td><td>Ok</td><td>ok</td></tr>
-<tr><td>35S+LTB+T35S C2</td><td>35S+ePDZ+VP16+T35S C1</td><td>35S+ePDZ+VP16+T35S C2</td><td></td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td></td></tr>
-</div></table>
-<p>Make colony PCR with 6 colonies of PhiC31:</p>
-<ul><li>DNA- </li>
-<li>JM1: 2 µl (dilution 1:10)</li>
-<li>JM2: 2 µl (dilution 1:10)</li>
-<li>Buffer Taq (with Mg): 2 µl</li>
-<li>dNTPs: 2.5 µl</li>
-<li>Taq: 0.5 µl</li>
-<li>H2O: 10 µl</li>
-<li>Program: 96ºC-2min; 96ºC-30min; 55ºC-30min; 72ºC-30min</li>
-</ul></ul>
-<p>Make a gel with the PCR but we did not see the correct bands.</p>
-<p>Repeat the colony PCR:</p>
-<ul><li>DNA- </li>
-<li>JM1: 2.5 µl (dilution 1:10)</li>
-<li>JM2: 2.5 µl (dilution 1:10)</li>
-<li>Buffer Taq (with Mg): 10 µl</li>
-<li>dNTPs: 2 µl</li>
-<li>Taq: 0.5 µl</li>
-<li>H2O: 7.5 µl</li>
-<li>Program: : 96ºC-10min; 96ºC-30min; 55ºC-30min; 72ºC-30min</li>
-</ul></ul>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:AsLOVpep+ePDZ; ?1</td><td>LacI:AsLOVpep+ePDZ; ?1</td><td>Gal4:AsLOVpep+ePDZ; ?1</td></tr>
-<tr><td>1 µl LexA:AsLOVpep; ?1</td><td>1 µl LacI:AsLOVpep; ?1</td><td>1 µl Gal4:AsLOVpep; ?1</td></tr>
-<tr><td>1 µl ePDZ; ?2</td><td>1 µl ePDZ; ?2</td><td>1 µl ePDZ; ?2</td></tr>
-<tr><td>1 µl BsmBI</td><td>1 µl BsmBI</td><td>1 µl BsmBI</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-<p>Refresh Agro cultures to agroinfiltrate:</p>
-<ul><li>PhiC31:RepPhiC31:GFP</li>
-<li>RepPhiC31:GFP</li>
-<li>BxbI:RepBxbI:GFP</li>
-<li>RepBxbI:GFP</li>
-<li>IFN (interferon)</li>
-<li>Sip-CH2</li>
-<li>Sip-CH2-CH3</li>
-<li>Pnos</li>
-<li>P19 (this culture ha 10ml of LB + 10 µl antibiotics + 5 µl culture)</li>
-</ul></ul>
-</br><h3 style="color:green">7 August 2015</h3>
-<p>Transformation into <i>Agrobacterium</i>:</p>
-<ul><li>35S:LTB:VP16:T35S</li>
-</ul></ul>
-<p>Transformation into E.coli and make petri dishes cultures:</p>
-<ul><li>LexA:AsLOVpep+ePDZ</li>
-<li>LacI:AsLOVpep+ePDZ</li>
-<li>Gal4:AsLOVpep+ePDZ</li>
-</ul></ul>
-<p>Make a gel with the colonies PCRs:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>C7</td><td>C8</td><td>C9</td><td>C10</td><td>C11</td><td>C12</td><td>C13</td><td>C14</td></tr>
-<tr><td>No</td><td>no</td><td>no</td><td>no</td><td>no</td><td>no</td><td>no</td><td>no</td></tr>
-</div></table>
-<p>There was no DNA, there is a problem with the cells or the procedure, it have to be revised.</p>
-<p>Ligation:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PhyC31; pUPD2</td></tr>
-<tr><td>3 µl PhiC31</td></tr>
-<tr><td>1 µl pUPD2</td></tr>
-<tr><td>1 µl BsmBI</td></tr>
-<tr><td>3.6 µl H2O</td></tr>
-</div></table>
-<p>Refresh agrobacterium cultures for tomorrow infiltration:</p>
-<ul><li>Sip-CH2</li>
-<li>Sip-CH2-CH3</li>
-<li>Pnos</li>
-<li>Red toggle (PIF6:PhyB:luc )</li>
-<li>Renilla</li>
-<li>Blue toggle (….:KDronpa:NDronpa:ren:luc)</li>
-</ul></ul>
-<ul><li>A new experiment was started:</li>
-<ul class="ul_2"><li>We are going to check again the recombinase BxbI and its reporter (negative control). </li>
-</ul></ul>
-<ul><li>Test the recombinase PhiC31. Due to that we did not obtain yet the complete recombinase, we will coinfiltrate the
-PhiC31 and the RepPhiC31:GFP following the same scheme as BxbI. 2 plants with 2 leafs, one of them with PhiC31 +
-RepPhiC31:GFP and the other with only RepPhiC31:GFP.</li>
-<li>Infiltration in 2 plants with 2 leafs each of them with interferon.</li>
-</ul></ul>
-<p>Measure f the ODs:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Construction</td><td>OD</td><td>Volume (ml)</td></tr>
-<tr><td>IFN</td><td>0.13</td><td>1.54</td></tr>
-<tr><td>RepBxbI:GFP</td><td>0.13</td><td>1.54</td></tr>
-<tr><td>BxbI:RepBxbI:GFP</td><td>0.33</td><td>0.61</td></tr>
-<tr><td>PhiC31</td><td>0.19</td><td>1.05</td></tr>
-<tr><td>RepPhiC31:GFP</td><td>0.22</td><td>0.91</td></tr>
-</div></table>
-</br><h3 style="color:green">8 August 2015</h3>
-<p>Transform the ligation into E.coli and make petri dishes cultures:</p>
-<ul><li>PhiC31; pUPD2.</li>
-</ul></ul>
-<ul><li>LexA:AsLOVpep+ePDZ (C1-C5)</li>
-<li>LacI:AsLOVpep+ePDZ (C1-C4)</li>
-<li>Gal4:AsLOVpep+ePDZ (C1-C4)</li>
-</ul></ul>
-<p>New experiment:</p>
-<p>It will be tested again the red toggle (PIF6:PhyB:luc + ren), the blue toggle (LacI:KDronpa:NDronpa:ren:luc), pnos
-(positive control to check the ratio renilla luciferasa) and the production of antirotavirus that are SIP rotavirus CH2
-and SIP rotavirus CH2-CH3.</p>
-<p>2 plants with 3 leafs ache one were infiltrated with pnos.</p>
-<p>The same with the red(4) and blue toggle(4) and sip rativurs I DON’T KNOW</p>
-<p>Measurement of the ODs:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Construction</td><td>OD</td><td>Volume (ml)</td></tr>
-<tr><td>Sip-CH2</td><td>0.04</td><td>6.667</td></tr>
-<tr><td>Sip-CH2-CH3</td><td>0.04</td><td>6.667</td></tr>
-<tr><td>Red toggle (PIF6:PhyB:luc)</td><td>0.09</td><td>15</td></tr>
-<tr><td>Blue toggle (LacI:KDronpa:NDronpa:ren:luc)</td><td>0.09</td><td>15.00</td></tr>
-<tr><td>Renilla</td><td>0.04</td><td>6.667</td></tr>
-<tr><td>Pnos</td><td>0.04</td><td>6.667</td></tr>
-</div></table>
-</br><h3 style="color:green">9 August 2015</h3>
-<p>Make a colony PCRs with the 10 white colonies of PhiC31 that grow in the petri dishes.</p>
-<ul><li>DNA- colony</li>
-<li>JM1: 2 µl (dilution 1:10)</li>
-<li>JM2: 2 µl (dilution 1:10)</li>
-<li>Buffer Taq (with Mg): 2 µl</li>
-<li>dNTPs: 2.5 µl</li>
-<li>Taq: 0.5 µl</li>
-<li>H2O: 1 µl</li>
-</ul></ul>
-<p>Minipreps of the liquid cultures:</p>
-<ul><li>LexA:AsLOVpep+ePDZ (C1-C4) C5 has turn into blue color.</li>
-<li>LacI:AsLOVpep+ePDZ (C1-C4)</li>
-<li>Gal4:AsLOVpep+ePDZ (C1-C4)</li>
-</ul></ul>
-<p>Digestion of the minipreps:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:AsLOVpep+ePDZ</td><td>BamHI</td><td>6674, 4309</td></tr>
-<tr><td>LacI:AsLOVpep+ePDZ</td><td>BamHI</td><td>6674, 5041</td></tr>
-<tr><td>Gal4:AsLOVpep+ePDZ</td><td>BamHI</td><td>6674, 4270</td></tr>
-</div></table>
-<p>Make the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:AsLOVpep+ePDZ (C1)</td><td>LexA:AsLOVpep+ePDZ (C2)</td><td>LexA:AsLOVpep+ePDZ (C3)</td><td>LexA:AsLOVpep+ePDZ
-(C4)</td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>oLacI:AsLOVpep+ePDZ (C1)</td><td>LacI:AsLOVpep+ePDZ (C2)</td><td>LacI:AsLOVpep+ePDZ (C3)</td><td>LacI:AsLOVpep
-+ePDZ (C4)</td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td>ok</td></tr>
-<tr><td>Gal4:AsLOVpep+ePDZ (C1)</td><td>Gal4:AsLOVpep+ePDZ (C2)</td><td>Gal4:AsLOVpep+ePDZ (C3)</td><td>Gal4:AsLOVpep+ePDZ
-(C4)</td></tr>
-<tr><td>Ok</td><td>ok</td><td>ok</td><td>Ok</td></tr>
-</div></table>
-<p>We keep in our inventory the colony C1 of each construction</p>
-<p>Make a gel of the colonies PCRs of PhiC31: we did not observed any DNA. Still can’t fix the problem.	</p>
-<p>Make liquid culture of renilla and PIF6:phyB:luc in <i>Agrobacterium</i> because the last time that we did an
-experiment they have grown slowly.</p>
-<p>Store in the 4ºC fridge an agrobacterium culture with P19.</p>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:AsLOVpep+ePDZ+ren; ?1</td><td>LacI:AsLOVpep+ePDZ+ren; ?1</td><td>Gal4:AsLOVpep+ePDZ+ren; ?1</td></tr>
-<tr><td>1µl LexA:AsLOVpep+ePDZ</td><td>1µl LacI:AsLOVpep+ePDZ</td><td>1µl Gal4:AsLOVpep+ePDZ</td></tr>
-<tr><td>1 µl renilla (159)</td><td>1 µl renilla (159)</td><td>1 µl renilla (159)</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
-</br><h3 style="color:green">10 August 2015</h3>
-<p>Transform into E.coli this ligations and make petri dishes cultures:</p>
-<ul><li>LexA:AsLOVpep+ePDZ+ren; ?1</li>
-<li>LacI:AsLOVpep+ePDZ+ren; ?1</li>
-<li>Gal4:AsLOVpep+ePDZ+ren; ?1</li>
-<li>(we add into the tubes X-gal and IPTG)</li>
-</ul></ul>
-<p>Make liquid culture of 11 colonies of PhiC31 due to that this construction was giving us problems to obtain.</p>
-<p>Refresh the agrobacterium cultures of:</p>
-<ul><li>BxbI:Rep:BxbI:GFP</li>
-<li>Rep:BxbI:GFP</li>
-<li>PhiC31</li>
-<li>RepPhiC31:GFP</li>
-<li>P19</li>
-<li>Citoplasm</li>
-<li>Integrase</li>
-<li>Dsred</li>
-<li>GFP</li>
-</ul></ul>
-<p>Take the samples of the agroinfiltrated plants that were in darkness for 2 days and make discs of them to change the
-conditions.</p>
-<p>Make liquid culture of:</p>
-<ul><li>LexA:AsLOVpep+ePDZ+ren (C1 and C2)</li>
-<li>LacI:AsLOVpep+ePDZ+ren (C1-C4)</li>
-<li>Gal4:AsLOVpep+ePDZ+ren (C1 and C2)</li>
-<li>(we add X-Gal and IPTG because they  are small)</li>
-</ul></ul>
-</br><h3 style="color:green">11 August 2015</h3>
-<p>Primers have arrived, they have been resuspended. They were used to eliminate the recognitions sites of the enzymes in
-BioBricks. This will make our constructions ready to be send to the iGEM</p>
-<p>Minipreps of the liquid cultures done yesterday:</p>
-<ul><li>PhiC31 (C6-C16)</li>
-<li>LacI:AsLOVpep+ePDZ+ren (C1-C4)</li>
-<li>Gal4:AsLOVpep+ePDZ+ren (C1 and C2)</li>
-<li>(LexA:AsLOVpep+ePDZ+rencolonies were all blue)</li>
-</ul></ul>
-<p>Make PCRs with all the primers and constructions:</p>
-<p>All of them follow the same composition which is:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>10 µl </td><td>Buffer HF</td></tr>
-<tr><td>26.5 µl</td><td>H2O</td></tr>
-<tr><td>2 µl</td><td>dNTPs</td></tr>
-<tr><td>0.5 µl</td><td>Taq Phusion</td></tr>
-<tr><td>1 µl </td><td>DNA (dilution 1:10)</td></tr>
-<tr><td>2.5 µl</td><td>Primer forward (F) (dilution 1:10)</td></tr>
-<tr><td>2.5 µl</td><td>Primer reverse (R) (dilution 1:10)</td></tr>
-</div></table>
-<p>*green ones are the only specify.</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>IFN (1)</td><td>IFN (2)</td><td>AsLOVpep (1)</td><td>AsLOVpep (2)</td></tr>
-<tr><td>IFN</td><td>IFN</td><td>AsLOVpep</td><td>AsLOVpep</td></tr>
-<tr><td>Mys int F</td><td>IFN domBB R</td><td>AsLOVpep F</td><td>AsLOVpep Fint</td></tr>
-<tr><td>Mys int R</td><td>IFN domBB F</td><td>AsLOVpep Rint</td><td>AsLOVpep R</td></tr>
-<tr><td>AsLOVpep (nested)</td><td>PhiC31 (1)</td><td>PhiC31 (2)</td><td>PhiC31 (3)</td></tr>
-<tr><td>AsLOVpep</td><td>PhiC31</td><td>PhiC31</td><td>PhiC31</td></tr>
-<tr><td>AsLOVpep nested</td><td>PhiC31 Fint 1</td><td>PhiC31 Fint 2</td><td>PhiC31 Fint 3</td></tr>
-<tr><td>AsLOVpep</td><td>PhiC31 Rint 2</td><td>PhiC31 Rint 3</td><td>PhiC31 R</td></tr>
-<tr><td>PhiC31</td></tr>
-<tr><td>PhiC31</td></tr>
-<tr><td>PhiC31 F</td></tr>
-<tr><td>PhiC31 Rint</td></tr>
-</div></table>
-<p>Digestions of the minipreps:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PhiC31</td><td>NotI</td><td>2046, 1899</td></tr>
-<tr><td>LacI:AsLOVpep+ePDZ+ren </td><td>EcoRI</td><td>6345, 8798</td></tr>
-<tr><td>Gal4:AsLOVpep+ePDZ+ren </td><td>EcoRI</td><td>6345, 9569</td></tr>
-</div></table>
-<p>Make the gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>PhiC31 (C6)</td><td>C7…C16</td><td>LacI:AsLOVpep:ePDZ:ren (C1)</td><td>C2</td><td>C3…C4</td></tr>
-<tr><td>no</td><td>no</td><td>ok</td><td>no</td><td>ok</td></tr>
-<tr><td>Gal4:AsLOVpep+ePDZ+ren (C1)</td><td>Gal4:AsLOVpep+ePDZ+ren (C2)</td><td></td><td></td></tr>
-<tr><td>ok</td><td>ok</td><td></td><td></td></tr>
-</div></table>
-<p>Mesurement of the ODs:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Citoplasm</td><td>0.21</td><td>7.35 ml</td></tr>
-<tr><td>RepPhiC31</td><td>0.26</td><td>9.1ml</td></tr>
-<tr><td>35S:LTB:T35S</td><td>0.27</td><td>9.45ml</td></tr>
-<tr><td>PhiC31</td><td>0.27</td><td>9.45ml</td></tr>
-<tr><td>GFP</td><td>0.20</td><td>10ml</td></tr>
-<tr><td>RepBxbI</td><td>0.33</td><td>11.55ml</td></tr>
-<tr><td></td><td></td></tr>
-<tr><td>PsinATG:RepBxbI:GFP</td><td>0.36</td><td>12.6ml</td></tr>
-<tr><td>PhiC31</td><td>0.34</td><td>11.9ml</td></tr>
-<tr><td>DsRed</td><td>0.26</td><td>9.1ml</td></tr>
-<tr><td>P19</td><td>0.28</td><td>9.8ml</td></tr>
-<tr><td></td><td></td></tr>
-</div></table>
-</br><h3 style="color:green">12 August 2015</h3>
-<p>New digestions to check if the negative control constructions are correct and we can transformed it in agro</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>OpLexA:luc:SF:ren</td><td>EcoRI</td><td>6345, 7274</td></tr>
-<tr><td>Op:UAS:luc:SF:ren</td><td>EcoRI</td><td>6345, 7096</td></tr>
-<tr><td>OpEtr8.luc:SF:ren</td><td>EcoRI</td><td>6345, 7294</td></tr>
-</div></table>
-<p>Gel:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>Op:UAS:luc:SF:ren C1</td><td>Op:UAS:luc:SF:ren C2</td><td>Op:UAS:luc:SF:ren C3</td><td>OpEtr8.luc:SF:ren</td></tr>
-<tr><td>no</td><td>no</td><td>no</td><td>no</td></tr>
-<tr><td>OpLexA:luc:SF:ren C1</td><td>OpLexA:luc:SF:ren C2</td><td>Partner dna</td><td>Partner dna</td></tr>
-<tr><td>no</td><td>no</td><td></td></tr>
-</div></table>
-<p>Transform in Agro and make petri dishes cultures:</p>
-<ul><li>LexA:AsLOVpep:ePDZ</li>
-<li>Gal4:AsLOVpep:ePDZ</li>
-<li>LacI:AsLOVpep:ePDZ</li>
-<li>LexA:PIF6:phyB:VP16</li>
-<li>Gal4:PIF6:phyB:VP16</li>
-<li>LacI:PIF6:phyB:VP16</li>
-<li>All of them are in ?1.</li>
-</ul></ul>
-<p>Ligations:</p>
-<div class="table-wrapper"><table class="alt">
-<tr><td>LexA:AsLOVpep:ePDZ+ren; ?1</td><td>Gal4:AsLOVpep:ePDZ:ren+OpUAS:luc; ?1</td><td>LacI:AsLOVpep:ePDZ:ren+OpLacI:luc;
-?1</td></tr>
-<tr><td>1 µl LexA:AsLOVpep:ePDZ</td><td>1 µl Gal4:AsLOVpep:ePDZ:ren</td><td>1 µl LacI:AsLOVpep:ePDZ</td></tr>
-<tr><td>1 µl renilla (159)</td><td>1 µl OpUAS:luc</td><td>1 µl OpLacI:luc</td></tr>
-<tr><td>1 µl ?1</td><td>1 µl ?1</td><td>1 µl ?1</td></tr>
-<tr><td>4.6 µl H2O</td><td>4.6 µl H2O</td><td>4.6 µl H2O</td></tr>
-</div></table>
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