Difference between revisions of "Team:Pasteur Paris/Experiments"
Alma.chapet (Talk | contribs) |
Alma.chapet (Talk | contribs) |
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</p> | </p> | ||
− | < | + | <h3> Ligation</h3> |
<p> | <p> | ||
<ul> | <ul> | ||
Line 107: | Line 107: | ||
<h3> MiniPrep </h3> | <h3> MiniPrep </h3> | ||
+ | <h4> 1) Bacterial Culture Growth</h4> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li> Pick a single colony from a freshly streaked selective plate and inoculate a starter culture of 2–5 ml LB medium containing the appropriate selective antibiotic. </li> | ||
+ | <li> Incubate for 8 h at 37°C with vigorous shaking (~300 rpm). </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | <h4> 2) Plasmid purification</h4> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li>Dilute the starter culture 1/500 to 1/1000 into selective LB medium. </li> | ||
+ | <li>Grow at 37°C for 12–16 h with vigorous shaking (approx. 300 rpm). </li> | ||
+ | <li>Centrifuge at 6000 x g for 15 min at 4°C. </li> | ||
+ | <li>Resuspend the bacterial pellet in 4 ml Buffer P1. </li> | ||
+ | <li>Add 4 ml Buffer P2, mix thoroughly by vigorously inverting the sealed tube 4–6 times </li> | ||
+ | <li>Incubate at room temperature (15–25°C) for 5 min. </li> | ||
+ | <li>Add 4 ml of chilled Buffer P3, mix immediately and thoroughly by vigorously inverting 4–6 times. </li> | ||
+ | <li>Incubate on ice for 15 min. </li> | ||
+ | <li>Centrifuge at ≥20,000 x g for 30 min at 4°C. Remove supernatant containing plasmid DNA promptly. </li> | ||
+ | <li>Centrifuge the supernatant again at ≥20,000 x g for 15 min at 4°C. Remove supernatant containing plasmid DNA promptly. </li> | ||
+ | <li>Equilibrate a QIAGEN-tip 100 by applying 4 ml Buffer QBT, and allow the column to empty by gravity flow. </li> | ||
+ | <li>Apply the supernatant from step 8 to the QIAGEN-tip and allow it to enter the resin by gravity flow. </li> | ||
+ | <li>Wash the QIAGEN-tip with 2x10ml BufferQC. </li> | ||
+ | <li>Elute DNA with 5ml BufferQF. </li> | ||
+ | <li>Collect the eluate in a 15 ml or 50ml tube. </li> | ||
+ | <li>Add 3.5 ml (0.7 volumes) room-temperature isopropanol to the eluted DNA. </li> | ||
+ | <li>Mix and centrifuge immediately at ≥15,000 x g for 30 min at 4°C. </li> | ||
+ | <li>Carefully decant the supernatant. </li> | ||
+ | <li>Air-dry the pellet for 5–10 min, and redissolve the DNA in a suitable volume of TE 8.1 Buffer. </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <h3> Stab Cultures</h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li>Prepare and autoclave 0.7% LB agar (standard LB medium containing 7 g/liter agar). </li> | ||
+ | <li>Cool the LB agar to below 50°C (when you can hold it comfortably) and add the appropriate antibiotic(s). While still liquid, add 1 ml agar to a 2 ml screw-cap vial under sterile conditions, then leave to solidify.</li> | ||
+ | <li>Using a sterile straight wire, pick a single colony from a freshly grown plate and stab it deep down into the soft agar several times. </li> | ||
+ | <li>Incubate the vial at 37°C for 8–12 h leaving the cap slightly loose. </li> | ||
+ | <li>Seal the vial tightly and store in the dark, preferably at 4°C. </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | <h3> MidiPrep </h3> | ||
<h4> 1) Bacterial Culture Growth</h4> | <h4> 1) Bacterial Culture Growth</h4> | ||
<p> | <p> | ||
Line 133: | Line 179: | ||
<li>Let stand for 1 min. </li> | <li>Let stand for 1 min. </li> | ||
<li>Centrifuge for 1 min. </li> | <li>Centrifuge for 1 min. </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | <h3>Transformation in chemically competent E.coli DH5-⍺ </h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li> Thaw out on ice one tube of chemically competent E.coli DH5-α. </li> | ||
+ | <li> Place 50µL of cells in a pre-chilled MicroCentrifuge tube. </li> | ||
+ | <li> Refreeze any unused cells. </li> | ||
+ | <li>Add 1-10ng of DNA to the cells and mix gently. Do not mix by pipetting up and down.</li> | ||
+ | <li> Incubate on ice for 30 min. </li> | ||
+ | <li> Heat shock the cells for 40s in a 42°C water bath. </li> | ||
+ | <li> Place the tubes on ice for 3 minutes. </li> | ||
+ | <li> Add 700µl of prewarmed (37°C) SOC medium (Invitrogen NO 15544-034)</li> | ||
+ | <li> Incubate at 37°C for 40 min at 200 rpm. </li> | ||
+ | <li>Spread 200µL of transformed cells on the appropriate medium.</li> | ||
+ | <li>Incubate overnight at 37°C</li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | <h3> Agarose Gel Electrophoresis </h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li>Prepare the different dilutions of TAE Buffer (50X, 1X, 0.5X) </li> | ||
+ | <li>Agarose gel preparation : </li> | ||
+ | <ul> | ||
+ | <li>Weigh the agarose (Invitrogen Ref 16500-500) depending on the size of your DNA.</li> | ||
+ | <li>Dissolve it in the appropriate amount of TAE Buffer (1X). </li> | ||
+ | <li>Heat the preparation in the microwave until the agarose is dissolved. </li> | ||
+ | <li>Cool the preparation by letting cool water flow against the Erlenmeyer until there is no evaporation. </li> | ||
+ | <li>Add 1 drop of BET (Eurobio Ref GEPBET02-AF) under the extraction hood. Mix gently. </li> | ||
+ | <li>Pour the solution in the casting tray and remove any bubbles. </li> | ||
+ | <li>Place the combs in the casting tray and let it rest until the gel is solid. </li> | ||
+ | <li>Carefully remove the combs from the gel </li> | ||
+ | </ul> | ||
+ | <li>Place the agarose gel in the electrophoresis apparatus filled with TAE buffer (0,5X). </li> | ||
+ | <li>Gel loading: </li> | ||
+ | <ul> | ||
+ | <li>Load 2µl of DNA ladder in the first and eventually the last well. </li> | ||
+ | <li>Load each well with the appropriate amount of DNA. </li> | ||
+ | </ul> | ||
+ | <li>Close the electrophoresis unit and run the gel for 1 hour at 130V and 7mA. </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <h3> </h3> | ||
+ | <p> All the following steps take place under sterile conditions and on ice</p> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li>Inoculate 500mL of L-broth with 1/100 volume of a fresh overnight E. coli BAP1 culture. </li> | ||
+ | <li>Grow the cells at 37 °C at 300 rpm. </li> | ||
+ | <li>Chill cells on ice for about 20 min. </li> | ||
+ | <li>Transfer the cells to a cold centrifuge bottle and spin at 4000 x g for 15 minutes at 4 °C. </li> | ||
+ | <li>Carefully pour off and discard the supernatant. It is better to sacrifice a few cells than to leave supernatant behind. </li> | ||
+ | <li>Gently re-suspend the pellet in 500 ml of ice-cold glycerol (10%). </li> | ||
+ | <li>Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant. </li> | ||
+ | <li>Re-suspend the pellet in 250 ml of ice-cold glycerol (10%). </li> | ||
+ | <li>Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant. </li> | ||
+ | <li>Re-suspend the pellet in ~ 20 ml of ice-cold glycerol (10%). </li> | ||
+ | <li>Transfer to a 30 ml sterile Oakridge tube. </li> | ||
+ | <li>Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant. </li> | ||
+ | <li>Re-suspend the cell pellet in a final volume of 2 ml of ice-cold 10% glycerol. The cell concentration should be about 3 x 1010 cells/ml.</li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <h3> </h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <h3> </h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | |||
+ | <h3> </h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
+ | <li> </li> | ||
</ul> | </ul> | ||
</p> | </p> |
Revision as of 13:34, 18 September 2015
Polymerase Chain Reaction
1) PCR Amplification using Takara Ex Taq DNA polymerase
- In a 0.2ml tube, set up the following reaction: tableau
- Set up the following cycles in a PCR machine
- Initial denaturation : 94°C for 30 sec
- 30 cycles :
- 94°C for 30s
- 55°C - 65°C for 1 min depending on your annealing temperature
- 72°C 0.5-1 min per kb
- Final extension: 72°C for 5min.
2) PCR Amplification using Phusion DNA polymerase
- In a 0.2ml tube, set up the following reaction: tableau
- Set up the following cycles in a PCR machine
- Initial denaturation : 98°C for 30 sec
- 30 cycles :
- 94°C for 5-10s
- 45°C - 72°C for 10 to 30s depending on your annealing temperature
- 72°C for 15-30s per kb
- Final extension: 72°C for 5min.
3) PCR Amplification using Q5 High Fidelity Master Mix DNA polymerase
- In a 0.2ml tube, set up the following reaction: tableau
- Set up the following cycles in a PCR machine
- Initial denaturation : 98°C for 30 sec
- 30 cycles :
- 94°C for 5-10s
- 45°C - 72°C for 10 to 30s depending on your annealing temperature
- 72°C for 20-30s per kb
- Final extension: 72°C for 2min.
Enzymatic Digestion
1) Single restriction enzyme digestion
- In a MicroCentrifuge tube, set up the following reaction on ice: tableau
- Pipette up and down to homogenize the solution.
- Quick spin in a MicroCentrifuge (5s).
- Incubation at 37°C for 1h.
- Heat inactivation for 20min at 80°C. Optional
- Add the phosphatase: Add 1 unit of Shrimp Alkaline Phosphatase for each pmol of phosphate end.
- Incubate for 30min at 37°C.
- Inactivate the phosphatase at 65°C for 15 min.
2) Double digestion
- In a MicroCentrifuge tube, set up the following reaction on ice: tableau
- Pipette up and down to homogenize the solution.
- Quick spin in a MicroCentrifuge (5s).
- Incubation at 37°C for 1h.
- Heat inactivation for 20min at 80°C. Optional
- Add the phosphatase: Add 1 unit of Shrimp Alkaline Phosphatase for each pmol of phosphate end.
- Incubate for 30min at 37°C.
- Inactivate the phosphatase at 65°C for 15 min.
Ligation
- Thaw the T4 DNA Ligase Buffer and DNA at room temperature.
- Set up the following reaction in a microcentrifuge tube on ice : tableau
- Gently mix the reaction by pipetting up and down
- Quick spin in a MicroCentrifuge (5s).
- For cohesive ends, incubation at 16°C for 1h.
- Heat inactivation for 10min at 65°C.
MiniPrep
1) Bacterial Culture Growth
- Pick a single colony from a freshly streaked selective plate and inoculate a starter culture of 2–5 ml LB medium containing the appropriate selective antibiotic.
- Incubate for 8 h at 37°C with vigorous shaking (~300 rpm).
2) Plasmid purification
- Dilute the starter culture 1/500 to 1/1000 into selective LB medium.
- Grow at 37°C for 12–16 h with vigorous shaking (approx. 300 rpm).
- Centrifuge at 6000 x g for 15 min at 4°C.
- Resuspend the bacterial pellet in 4 ml Buffer P1.
- Add 4 ml Buffer P2, mix thoroughly by vigorously inverting the sealed tube 4–6 times
- Incubate at room temperature (15–25°C) for 5 min.
- Add 4 ml of chilled Buffer P3, mix immediately and thoroughly by vigorously inverting 4–6 times.
- Incubate on ice for 15 min.
- Centrifuge at ≥20,000 x g for 30 min at 4°C. Remove supernatant containing plasmid DNA promptly.
- Centrifuge the supernatant again at ≥20,000 x g for 15 min at 4°C. Remove supernatant containing plasmid DNA promptly.
- Equilibrate a QIAGEN-tip 100 by applying 4 ml Buffer QBT, and allow the column to empty by gravity flow.
- Apply the supernatant from step 8 to the QIAGEN-tip and allow it to enter the resin by gravity flow.
- Wash the QIAGEN-tip with 2x10ml BufferQC.
- Elute DNA with 5ml BufferQF.
- Collect the eluate in a 15 ml or 50ml tube.
- Add 3.5 ml (0.7 volumes) room-temperature isopropanol to the eluted DNA.
- Mix and centrifuge immediately at ≥15,000 x g for 30 min at 4°C.
- Carefully decant the supernatant.
- Air-dry the pellet for 5–10 min, and redissolve the DNA in a suitable volume of TE 8.1 Buffer.
Stab Cultures
- Prepare and autoclave 0.7% LB agar (standard LB medium containing 7 g/liter agar).
- Cool the LB agar to below 50°C (when you can hold it comfortably) and add the appropriate antibiotic(s). While still liquid, add 1 ml agar to a 2 ml screw-cap vial under sterile conditions, then leave to solidify.
- Using a sterile straight wire, pick a single colony from a freshly grown plate and stab it deep down into the soft agar several times.
- Incubate the vial at 37°C for 8–12 h leaving the cap slightly loose.
- Seal the vial tightly and store in the dark, preferably at 4°C.
MidiPrep
1) Bacterial Culture Growth
- Pick a single colony from a freshly streaked selective plate and inoculate a culture of 1–5 ml LB medium containing the appropriate selective antibiotic.
- Incubate for 12–16 h at 37°C with vigorous shaking.
- Centrifugation at > 8000 rpm (6800 x g) in MicroCentrifuge for 3 min at room temperature (15–25°C).
- Remove all traces of supernatant by inverting the open centrifuge tube until all medium has been drained.
2) Plasmid purification
- Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer to a micro- centrifuge tube.
- Add 250 μl Buffer P2 and mix thoroughly by inverting the tube 4–6 times.
- Add 350 μl Buffer N3 and mix immediately and thoroughly by inverting the tube 4–6 times.
- Centrifuge for 10 min at 13,000 rpm in a MicroCentrifuge.
- Apply the supernatants to the QIAprep spin column by decanting or pipetting.
- Centrifuge for 30–60 s. Discard the flow-through.
- Recommended: Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30–60 s. Discard the flow-through.
- Add 0.75 ml Buffer PE and centrifuge for 30–60 s.
- Discard the flow-through, and centrifuge at full speed for an additional 1 min.
- Place the QIAprep column in a clean 1.5 ml microcentrifuge tube.
- Add 50 μl Buffer EB (10 mM Tris·Cl, pH 8.5) or water to the center of each QIAprep spin column.
- Let stand for 1 min.
- Centrifuge for 1 min.
Transformation in chemically competent E.coli DH5-⍺
- Thaw out on ice one tube of chemically competent E.coli DH5-α.
- Place 50µL of cells in a pre-chilled MicroCentrifuge tube.
- Refreeze any unused cells.
- Add 1-10ng of DNA to the cells and mix gently. Do not mix by pipetting up and down.
- Incubate on ice for 30 min.
- Heat shock the cells for 40s in a 42°C water bath.
- Place the tubes on ice for 3 minutes.
- Add 700µl of prewarmed (37°C) SOC medium (Invitrogen NO 15544-034)
- Incubate at 37°C for 40 min at 200 rpm.
- Spread 200µL of transformed cells on the appropriate medium.
- Incubate overnight at 37°C
Agarose Gel Electrophoresis
- Prepare the different dilutions of TAE Buffer (50X, 1X, 0.5X)
- Agarose gel preparation :
- Weigh the agarose (Invitrogen Ref 16500-500) depending on the size of your DNA.
- Dissolve it in the appropriate amount of TAE Buffer (1X).
- Heat the preparation in the microwave until the agarose is dissolved.
- Cool the preparation by letting cool water flow against the Erlenmeyer until there is no evaporation.
- Add 1 drop of BET (Eurobio Ref GEPBET02-AF) under the extraction hood. Mix gently.
- Pour the solution in the casting tray and remove any bubbles.
- Place the combs in the casting tray and let it rest until the gel is solid.
- Carefully remove the combs from the gel
- Place the agarose gel in the electrophoresis apparatus filled with TAE buffer (0,5X).
- Gel loading:
- Load 2µl of DNA ladder in the first and eventually the last well.
- Load each well with the appropriate amount of DNA.
- Close the electrophoresis unit and run the gel for 1 hour at 130V and 7mA.
All the following steps take place under sterile conditions and on ice
- Inoculate 500mL of L-broth with 1/100 volume of a fresh overnight E. coli BAP1 culture.
- Grow the cells at 37 °C at 300 rpm.
- Chill cells on ice for about 20 min.
- Transfer the cells to a cold centrifuge bottle and spin at 4000 x g for 15 minutes at 4 °C.
- Carefully pour off and discard the supernatant. It is better to sacrifice a few cells than to leave supernatant behind.
- Gently re-suspend the pellet in 500 ml of ice-cold glycerol (10%).
- Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant.
- Re-suspend the pellet in 250 ml of ice-cold glycerol (10%).
- Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant.
- Re-suspend the pellet in ~ 20 ml of ice-cold glycerol (10%).
- Transfer to a 30 ml sterile Oakridge tube.
- Centrifuge at 4000 x g for 15 minutes at 4 °C. Carefully pour off and discard the supernatant.
- Re-suspend the cell pellet in a final volume of 2 ml of ice-cold 10% glycerol. The cell concentration should be about 3 x 1010 cells/ml.
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