Difference between revisions of "Team:FAU Erlangen/Tour52"
Line 243: | Line 243: | ||
<ul> | <ul> | ||
<li>over night digestion golden gate insert 2 | <li>over night digestion golden gate insert 2 | ||
+ | </ul> | ||
+ | |||
<b>Ligation: TALE in Vector pUC19_2</b> | <b>Ligation: TALE in Vector pUC19_2</b> | ||
<ul> | <ul> | ||
<li>3.5x Mastermix | <li>3.5x Mastermix | ||
+ | </ul> | ||
<b>Plurification</b> | <b>Plurification</b> | ||
Line 252: | Line 255: | ||
<li>of vector 181 (linearazed) Ampr-Leu | <li>of vector 181 (linearazed) Ampr-Leu | ||
<li>DNA plurification kit | <li>DNA plurification kit | ||
+ | </ul> | ||
<b>ReTrafo</b> | <b>ReTrafo</b> | ||
<ul> | <ul> | ||
<li>of K801000 iGEM vector Ampr-Ura | <li>of K801000 iGEM vector Ampr-Ura | ||
+ | </ul> | ||
<b>Miniprep EC insert</b> | <b>Miniprep EC insert</b> | ||
<ul> | <ul> | ||
− | <li>Miniscreen protocol, resuspend DNA in 40µl ddH2O | + | <li>Miniscreen protocol, resuspend DNA in 40µl ddH2O |
+ | </ul> | ||
<b>Digestion of EC</b> | <b>Digestion of EC</b> | ||
<ul> | <ul> | ||
− | + | <li>22.5 µl DNA | |
− | + | <li>3 µl Tango Buffer | |
− | + | <li>0.5 µl EcoRI | |
− | + | <li>4.5µl µl ddH2O | |
− | + | <li>1h at 37°C | |
− | + | <li>inactiviation: 20min at 65°C | |
+ | </ul> | ||
<b>Sequencing</b> | <b>Sequencing</b> | ||
Line 274: | Line 281: | ||
<li>10µl clone2 + 20µl ddH2O —> mutations | <li>10µl clone2 + 20µl ddH2O —> mutations | ||
<li>10µl clone5 + 20µl ddH2O —> mutations | <li>10µl clone5 + 20µl ddH2O —> mutations | ||
+ | </ul> | ||
<b>Transformation</b> | <b>Transformation</b> | ||
<ul> | <ul> | ||
<li>of Golden Gate (2) | <li>of Golden Gate (2) | ||
+ | </ul> | ||
<b>Fluid culture</b> | <b>Fluid culture</b> | ||
<ul> | <ul> | ||
− | <li> | + | <li>prepare 12 tubes with 2.5ml LB + Amp (4 for each insert) for the weekend |
+ | </ul> | ||
Line 292: | Line 302: | ||
<ul> | <ul> | ||
<li>of EC Plasmid-DNA + iGEM vector + 181 vector | <li>of EC Plasmid-DNA + iGEM vector + 181 vector | ||
+ | </ul> | ||
<b>Miniprep Golden Gate (2)</b> | <b>Miniprep Golden Gate (2)</b> | ||
Line 298: | Line 309: | ||
<li>protocoll „Miniscreens“ | <li>protocoll „Miniscreens“ | ||
<li>solve in 40µl ddH2O | <li>solve in 40µl ddH2O | ||
+ | </ul> | ||
<b>Digestion</b> | <b>Digestion</b> | ||
<ul> | <ul> | ||
<li>of Golden Gate (2) | <li>of Golden Gate (2) | ||
+ | </ul> | ||
<b>Agarose gel</b> | <b>Agarose gel</b> | ||
Line 308: | Line 321: | ||
<li>+ 5µl Loading Dye | <li>+ 5µl Loading Dye | ||
<li>complete digestion (30µl) | <li>complete digestion (30µl) | ||
+ | </ul> | ||
<b>Plurification</b> | <b>Plurification</b> | ||
<ul> | <ul> | ||
<li>EC1 + 2 —> plurification kit | <li>EC1 + 2 —> plurification kit | ||
+ | </ul> | ||
<b>Ligation</b> | <b>Ligation</b> | ||
<ul> | <ul> | ||
<li>EC2 ligation into 181 and iGEM | <li>EC2 ligation into 181 and iGEM | ||
+ | </ul> | ||
<b>Agarose gel</b> | <b>Agarose gel</b> | ||
<ul> | <ul> | ||
− | <li>2µl Golden Gate digestion sample + 0.5µl Loading Dye | + | <li>2µl Golden Gate digestion sample + 0.5µl Loading Dye |
+ | </ul> | ||
<b>Sequencing</b> | <b>Sequencing</b> | ||
<ul> | <ul> | ||
<li>Insert 2_2: 3µl + 17µl ddH2O | <li>Insert 2_2: 3µl + 17µl ddH2O | ||
+ | </ul> | ||
<b>Golden Gate (3)</b> | <b>Golden Gate (3)</b> | ||
<ul> | <ul> | ||
− | + | <li>T4 ligase buffer (10x): 2 µl | |
− | + | <li>BSA: 2 µl | |
− | + | <li>T4 Ligase: 1 µl | |
− | + | <li>BsmBI (Esp III): 0.5 µl | |
− | + | <li>TAL fragments: each 5.2 µl | |
− | + | <li>ddH2O ad 20 µl | |
− | + | <li>PCR Program 5 | |
− | + | </ul> | |
− | + | ||
Line 345: | Line 362: | ||
<ul> | <ul> | ||
<li>because golden gate was not optimal | <li>because golden gate was not optimal | ||
− | + | ||
− | + | <li>T4 ligase buffer (10x; new): 2 µl | |
− | + | <li>T4 Ligase: 1 µl | |
− | + | <li>BsmBI (Esp III): 0.5 µl | |
− | + | <li>Golden Gate reaction: each 10 µl | |
− | + | <li>ddH2O: 8.5 µl | |
− | + | <li>40' at room temperature | |
+ | </ul> | ||
<b>Digestion (3)</b> | <b>Digestion (3)</b> | ||
Line 358: | Line 376: | ||
<li>with BamHI and SacI | <li>with BamHI and SacI | ||
<li>Inactivation of the enzymes for 20 min at 80°C | <li>Inactivation of the enzymes for 20 min at 80°C | ||
+ | </ul> | ||
<b>Transformation</b> | <b>Transformation</b> | ||
<ul> | <ul> | ||
<li>of the ligation | <li>of the ligation | ||
+ | </ul> | ||
<b>Agarose gel</b> | <b>Agarose gel</b> | ||
Line 367: | Line 387: | ||
<li>of the digested Golden Gate reaction | <li>of the digested Golden Gate reaction | ||
<li>1/5 of the digestion with 1.5 µl Loading Dye | <li>1/5 of the digestion with 1.5 µl Loading Dye | ||
+ | </ul> | ||
<b>Sequencing</b> | <b>Sequencing</b> | ||
<ul> | <ul> | ||
<li>Clone 10 + Clone 11 of rpd3 | <li>Clone 10 + Clone 11 of rpd3 | ||
+ | </ul> | ||
<b>Fluid culture</b> | <b>Fluid culture</b> | ||
<ul> | <ul> | ||
<li>one white colony of the ReTrafo of the iGEM vector in 20ml LB-medium | <li>one white colony of the ReTrafo of the iGEM vector in 20ml LB-medium | ||
+ | </ul> | ||
<b>Ligation (3)</b> | <b>Ligation (3)</b> | ||
<ul> | <ul> | ||
<li>of the Golden Gate reaction into pUC19 | <li>of the Golden Gate reaction into pUC19 | ||
+ | </ul> | ||
Line 388: | Line 412: | ||
<ul> | <ul> | ||
<li>of the Golden Gate ligation | <li>of the Golden Gate ligation | ||
+ | </ul> | ||
<b>Mixi-Prep</b> | <b>Mixi-Prep</b> | ||
Line 393: | Line 418: | ||
<li>of the iGEM vector | <li>of the iGEM vector | ||
<li>protocol „mixi-prep“ | <li>protocol „mixi-prep“ | ||
+ | </ul> | ||
<b>Ligation</b> | <b>Ligation</b> | ||
Line 398: | Line 424: | ||
<li>of EC2-fragment into 181-vector | <li>of EC2-fragment into 181-vector | ||
<li>because there were no white colonies last time, we do a new ligation | <li>because there were no white colonies last time, we do a new ligation | ||
+ | </ul> | ||
<b>Fluid culture</b> | <b>Fluid culture</b> | ||
<ul> | <ul> | ||
<li>of 6 clones of EC2 + iGEM-vector | <li>of 6 clones of EC2 + iGEM-vector | ||
+ | </ul> | ||
<b>Transformation</b> | <b>Transformation</b> | ||
<ul> | <ul> | ||
<li>of the rpd3-ligation | <li>of the rpd3-ligation | ||
+ | </ul> | ||
Line 416: | Line 445: | ||
<li>of EC + iGEM-vector | <li>of EC + iGEM-vector | ||
<li>protocol „miniscreens“ | <li>protocol „miniscreens“ | ||
+ | </ul> | ||
<b>Transformation</b> | <b>Transformation</b> | ||
Line 421: | Line 451: | ||
<li>of EC2 + 181-vector ligation (of 15/07/07) | <li>of EC2 + 181-vector ligation (of 15/07/07) | ||
<li>and Golden Gate ligation (of 15/07/14) | <li>and Golden Gate ligation (of 15/07/14) | ||
+ | </ul> | ||
<b>Digestion</b> | <b>Digestion</b> | ||
<ul> | <ul> | ||
<li>of the mini-prep | <li>of the mini-prep | ||
+ | </ul> | ||
<b>Plating</b> | <b>Plating</b> | ||
<ul> | <ul> | ||
<li>of the transformation onto LB-plates containing ampicillin, XGal and IPTG | <li>of the transformation onto LB-plates containing ampicillin, XGal and IPTG | ||
+ | </ul> | ||
<b>Agarose gel</b> | <b>Agarose gel</b> | ||
Line 434: | Line 467: | ||
<li>of the digestion | <li>of the digestion | ||
<li>add 4µl of Loading Dye | <li>add 4µl of Loading Dye | ||
+ | </ul> | ||
Line 445: | Line 479: | ||
<li>first incubate 1h at 37°C with only SacI | <li>first incubate 1h at 37°C with only SacI | ||
<li>then add BamHI and incubate for another hour | <li>then add BamHI and incubate for another hour | ||
+ | </ul> | ||
<b>Digestion</b> | <b>Digestion</b> | ||
<ul> | <ul> | ||
<li>of the 181-vector, because there were only blue colonies on the plates | <li>of the 181-vector, because there were only blue colonies on the plates | ||
+ | </ul> | ||
<b>Fluid culture</b> | <b>Fluid culture</b> | ||
Line 454: | Line 490: | ||
<li>of rpd3 —> 12 clones | <li>of rpd3 —> 12 clones | ||
<li>and of 2 blue clones of EC + 181 to test them | <li>and of 2 blue clones of EC + 181 to test them | ||
+ | </ul> | ||
<b>Ligation</b> | <b>Ligation</b> | ||
Line 459: | Line 496: | ||
<li>of Golden Gate into pUC19 | <li>of Golden Gate into pUC19 | ||
<li>of EC into 181-vector | <li>of EC into 181-vector | ||
+ | </ul> | ||
Line 469: | Line 507: | ||
<li>of the fluid cultures from 15/07/17 | <li>of the fluid cultures from 15/07/17 | ||
<li>protocol „miniscreens“ | <li>protocol „miniscreens“ | ||
+ | </ul> | ||
<b>Transformation</b> | <b>Transformation</b> | ||
<ul> | <ul> | ||
<li>of the ligations from 15/07/17 | <li>of the ligations from 15/07/17 | ||
+ | </ul> | ||
<b>Digestion</b> | <b>Digestion</b> | ||
<ul> | <ul> | ||
<li>of the mini-preps | <li>of the mini-preps | ||
+ | </ul> | ||
<b>Agarose gel</b> | <b>Agarose gel</b> | ||
Line 483: | Line 524: | ||
<li>rpd3: 15µl with 3µl loading dye | <li>rpd3: 15µl with 3µl loading dye | ||
<li>EC/181: 25µl with 5µl loading dye | <li>EC/181: 25µl with 5µl loading dye | ||
+ | </ul> | ||
<b>Sequencing</b> | <b>Sequencing</b> | ||
<ul> | <ul> | ||
<li>of 2 rpd3 clones | <li>of 2 rpd3 clones | ||
+ | </ul> | ||
Line 497: | Line 540: | ||
<li>of 4 clones for Golden Gate | <li>of 4 clones for Golden Gate | ||
<li>and 4 clones of EC + 181 | <li>and 4 clones of EC + 181 | ||
+ | </ul> | ||
Line 507: | Line 551: | ||
<li>of the fluid cultures | <li>of the fluid cultures | ||
<li>protocol „miniscreens“ | <li>protocol „miniscreens“ | ||
+ | </ul> | ||
<b>Digestion</b> | <b>Digestion</b> | ||
<ul> | <ul> | ||
<li>of the mini-preps | <li>of the mini-preps | ||
+ | </ul> | ||
<b>Agarose Gel</b> | <b>Agarose Gel</b> | ||
Line 516: | Line 562: | ||
<li>of the digestion | <li>of the digestion | ||
<li>with 3µl loading dye | <li>with 3µl loading dye | ||
+ | </ul> | ||
<b>Overlap-PCR</b> | <b>Overlap-PCR</b> | ||
Line 521: | Line 568: | ||
<li>of rpd3 | <li>of rpd3 | ||
<li>PCR program of 15/06/30 | <li>PCR program of 15/06/30 | ||
+ | </ul> | ||
<b>Sequencing</b> | <b>Sequencing</b> | ||
<ul> | <ul> | ||
<li>of Golden Gate fragment 1 and 3 | <li>of Golden Gate fragment 1 and 3 | ||
+ | </ul> | ||
Line 534: | Line 583: | ||
<ul> | <ul> | ||
<li>of the overlap-PCR | <li>of the overlap-PCR | ||
+ | </ul> | ||
<b>Gel extraction</b> | <b>Gel extraction</b> | ||
<ul> | <ul> | ||
<li>with Qiagen Gel Extraction Kit | <li>with Qiagen Gel Extraction Kit | ||
+ | </ul> | ||
<b>Agarose gel | <b>Agarose gel | ||
<ul> | <ul> | ||
<li>to control the gel extraction | <li>to control the gel extraction | ||
+ | </ul> | ||
<b>Ligation</b> | <b>Ligation</b> | ||
Line 547: | Line 599: | ||
<li>of rpd3 into PCR/Blunt | <li>of rpd3 into PCR/Blunt | ||
<li>protocol of 15/06/30 | <li>protocol of 15/06/30 | ||
+ | </ul> | ||
{{FAU_Erlangen_footer}} | {{FAU_Erlangen_footer}} |
Revision as of 20:59, 18 September 2015
Contents
15/06/30
Primer/rpd3 sequence fragments:
- centrifugation (5'; 13,000rpm): RPD3 sequences and primer
- adjust forward and reverse primer to 100µM (ddH2O) ? working concentration: 5µM (10µl primer + 190µl ddH2O)
- adjust RPD3 fragments to 10ng/µl (TE buffer) ? mixing ? incubation (50°C, 20') ? mixing
PCR
- ddH2O: 28.5 µl
- rdp3 fragment 2.1: 1 µl
- rdp3 fragment 2.2: 1 µl
- dNTP: 4 µl
- Phusion-Polymerase: 0.5 µl
- Phusion-Buffer (5x): 10 µl
- Primer rpd3_fw (5µM): 2.5 µl
- Primer rpd3_rv (5µM): 2.5 µl
negative control:
- ddH2O: 30.5 µl
- dNTP: 4 µl
- Phusion-Polymerase: 0.5 µl
- Phusion-Buffer (5x): 10 µl
- Primer rpd3_fw (5µM): 2.5 µl
- Primer rpd3_rv (5µM): 2.5 µl
- PCR Program 1 + 2
- 10µl negativ control-sample + 2µl loading dye
- whole PCR tube sample + 8µl loading dye
- 130 V, 45 min
- cut out both 1718bp fragments
- weigh fragments: fragment PCR programm 1: 0.2g fragment PCR programm 2: 0.38g
DNA fragment extraction (protocol Qiagen gel extraction kit)
- eluate extracted DNA in 30µl ddH2O
- control 1%-Agarosegel: 3µl elution + 2µl loading dye
Ligation
- of rpd3 fragment (PCR program 2) into PCR Blunt/StuI
15/07/01
Transformation
- Transformation protocol 1
Golden Gate
- adjust TALE fragments to 10ng/µl (TE buffer) ? mixing ? incubation (50°C, 20') ? mixing
- each TAL two samples (? 6 samples)
- TALE
- 1. CMV127_1 + CMV127_2 + TALE-CD (= 2416 bp)
- 2. CMV191_1 + CMV191_2 + TALE-CD (= 2416 bp)
- 3. GGGT_1 + GGGT_2 + TALE-CD (= 2416 bp)
- long protocol in ligase buffer
- sample:
- T4 ligase buffer (10x): 2 µl
- BSA: 2 µl
- T4 Ligase: 1 µl
- BsmBI (Esp III): 0.5 µl
- 3 TAL fragments each: 5.2 µl
- ddH2O: ad 20 µl
- PCR Program 3
Vector pUC19
- concentration measurment (NanoDrop): ~ 3µg/µl
- digestion
Golden Gate part 2: control gel
- 10µl TALE sample (1, 2 or 3) + 2µl loading dye
- 1% Agarose-TAE-Gel
15/07/02
no white colonies
Transformation
- Transformation protocol 1 (Repetition rpd3)
Repetition pf T4 Ligation
- rpd3 fragment PCR programm 1
Golden Gate
- combine equal samples (6 samples ? 3 samples)
- add 0.5µl BsmBI to each sample, incubate 1h, 55°C
- add 0.5µl Ligase to each sample
- PCR Program 4
1% Agarose Gel
15/07/06
Gel extraction
- TALEs and pUC19 (protocol Qiagen gel extraction kit)
Concentration measurement (NonoDrop)
- pUC19: 0.9 ng/µl
- pUC19: 5.4 ng/µl
- TAL1: 2.5 ngµl
- TAL2: 2.0 ng/µl
- TAL3: 1.4 ng/µl
Ligation
- of TALE in pUC19
Fluid culture
- 12 test tubes: á 2ml LB medium with Kanamycin
- add one white colonie to each tube
- incubation: 300rpm, over night, 37°C
15/07/07
Transformation
- Transformation protocol 2 (3x TALE)
15/07/08
Digestion
- of rpd3
Fluid culture
- of TALE
- 6 test tubes: á 2ml LB medium with Kanamycin
- add one white colony to each tube (plate1: 2 colonies; plate2: 3colonies; plate3: 1 colony)
- incubation: 300rpm, over night, 37°C
Gel-electrophorese
- 15µl digestion probe + 3µl loading dye
Sequencing
- 10µl Klon7 + 20µl ddH2O (M13-RP, GATC IJ1672)
15/07/09
Golden Gate (2)
- T4 ligase buffer (10x): 2 µl
- BSA: 2 µl
- T4 Ligase: 1 µl
- BsmBI (Esp III): 0.5 µl
- TAL fragments: each 5.2 µl
- ddH2O ad 20 µl
- PCR Program 5
Miniprep (1)
- culture sample ? protocol „Miniscreens“
Digestion
- of the mini-prep
- with BamHI and SacI
Agarosegel (2)
- of the Golden Gate
Insert EC culture
- 3 clones, 2ml LB Ampr
Digestion (2)
- of the Golden Gate
15/07/10
Agarosegel (test) (2)
- over night digestion golden gate insert 2
Ligation: TALE in Vector pUC19_2
- 3.5x Mastermix
Plurification
- of vector 181 (linearazed) Ampr-Leu
- DNA plurification kit
ReTrafo
- of K801000 iGEM vector Ampr-Ura
Miniprep EC insert
- Miniscreen protocol, resuspend DNA in 40µl ddH2O
Digestion of EC
- 22.5 µl DNA
- 3 µl Tango Buffer
- 0.5 µl EcoRI
- 4.5µl µl ddH2O
- 1h at 37°C
- inactiviation: 20min at 65°C
Sequencing
- 10µl clone2 + 20µl ddH2O —> mutations
- 10µl clone5 + 20µl ddH2O —> mutations
Transformation
- of Golden Gate (2)
Fluid culture
- prepare 12 tubes with 2.5ml LB + Amp (4 for each insert) for the weekend
15/07/13
Digestion
- of EC Plasmid-DNA + iGEM vector + 181 vector
Miniprep Golden Gate (2)
- 4 samples of each insert
- protocoll „Miniscreens“
- solve in 40µl ddH2O
Digestion
- of Golden Gate (2)
Agarose gel
- of EC + 181 + iGEM vector
- + 5µl Loading Dye
- complete digestion (30µl)
Plurification
- EC1 + 2 —> plurification kit
Ligation
- EC2 ligation into 181 and iGEM
Agarose gel
- 2µl Golden Gate digestion sample + 0.5µl Loading Dye
Sequencing
- Insert 2_2: 3µl + 17µl ddH2O
Golden Gate (3)
- T4 ligase buffer (10x): 2 µl
- BSA: 2 µl
- T4 Ligase: 1 µl
- BsmBI (Esp III): 0.5 µl
- TAL fragments: each 5.2 µl
- ddH2O ad 20 µl
- PCR Program 5
15/07/14
Addition of ligase (3)
- because golden gate was not optimal
- T4 ligase buffer (10x; new): 2 µl
- T4 Ligase: 1 µl
- BsmBI (Esp III): 0.5 µl
- Golden Gate reaction: each 10 µl
- ddH2O: 8.5 µl
- 40' at room temperature
Digestion (3)
- of Golden Gate-reaction
- with BamHI and SacI
- Inactivation of the enzymes for 20 min at 80°C
Transformation
- of the ligation
Agarose gel
- of the digested Golden Gate reaction
- 1/5 of the digestion with 1.5 µl Loading Dye
Sequencing
- Clone 10 + Clone 11 of rpd3
Fluid culture
- one white colony of the ReTrafo of the iGEM vector in 20ml LB-medium
Ligation (3)
- of the Golden Gate reaction into pUC19
15/07/15
Transformation
- of the Golden Gate ligation
Mixi-Prep
- of the iGEM vector
- protocol „mixi-prep“
Ligation
- of EC2-fragment into 181-vector
- because there were no white colonies last time, we do a new ligation
Fluid culture
- of 6 clones of EC2 + iGEM-vector
Transformation
- of the rpd3-ligation
15/07/16
Mini-Prep
- of EC + iGEM-vector
- protocol „miniscreens“
Transformation
- of EC2 + 181-vector ligation (of 15/07/07)
- and Golden Gate ligation (of 15/07/14)
Digestion
- of the mini-prep
Plating
- of the transformation onto LB-plates containing ampicillin, XGal and IPTG
Agarose gel
- of the digestion
- add 4µl of Loading Dye
15/07/17
Digestion
- of the Golden Gate reaction (of 15/07/13), because no colonies grew
- first incubate 1h at 37°C with only SacI
- then add BamHI and incubate for another hour
Digestion
- of the 181-vector, because there were only blue colonies on the plates
Fluid culture
- of rpd3 —> 12 clones
- and of 2 blue clones of EC + 181 to test them
Ligation
- of Golden Gate into pUC19
- of EC into 181-vector
15/07/20
Mini-prep
- of the fluid cultures from 15/07/17
- protocol „miniscreens“
Transformation
- of the ligations from 15/07/17
Digestion
- of the mini-preps
Agarose gel
- of the digestion
- rpd3: 15µl with 3µl loading dye
- EC/181: 25µl with 5µl loading dye
Sequencing
- of 2 rpd3 clones
15/07/22
Fluid culture
- of 4 clones for Golden Gate
- and 4 clones of EC + 181
15/07/23
Mini-prep
- of the fluid cultures
- protocol „miniscreens“
Digestion
- of the mini-preps
Agarose Gel
- of the digestion
- with 3µl loading dye
Overlap-PCR
- of rpd3
- PCR program of 15/06/30
Sequencing
- of Golden Gate fragment 1 and 3
15/07/24
Agarose gel
- of the overlap-PCR
Gel extraction
- with Qiagen Gel Extraction Kit
Agarose gel
- to control the gel extraction
<b>Ligation
- of rpd3 into PCR/Blunt
- protocol of 15/06/30