Paris/July 14
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Revision as of 16:27, 14 July 2007 by David.bikard (Talk | contribs)
What to do ?
- Remove the plate of the transduction experiment and the transformation ones from the 37°C incubator (Upper-left shelf): If it has worked and if someones comes on Sunday:
- isolation of the clones from the transduction on petri-dishes (LB+DAP+Erm+Citrate)
- LB + antibio culture of the transformants (to make a glycerol stock and to do MiniPreps)
- Make a gel (0.8%) and migrate the PCR products
- Purify them
- Do the assembly PCR
If enough time (we can also wait to have the plasmids to do everything at the same time):
- Digestion of the purifications products with appropriate enzymes
- Purification
What has been done
- Several colonies of transduced MG1655 are obtained (transduction from dapA- strain w121):
- Isolation of 10 different colonies on LB Citrate Erythro DAP plates
PCRs
PCR : Lox71-FtsA-FtsZ-1 | ||
---|---|---|
Name | Lox71-FtsA-FtsZ-1 | |
Annealing T° | 55°C | |
Time of elongation | 2m00' | |
Number of Cycles | 30 | |
Buffer | 5x 10µL | |
MgCl2 | 10µM 0µL | |
dNTP | 10µM 1µL | |
oligoF | 3 Lox71-FtsA-F | 10µM 2.5µL |
oligoR | 4 DEcoR1-FtsZ-R | 10µM 2.5µL |
water | 34µL | |
polymerase | Phusion 0.5µL | |
DNA | toughpick in glycerol stock of MG1655 |
PCR : FtsZ-2 | ||
---|---|---|
Name | FtsZ-2 | |
Annealing T° | 55°C | |
Time of elongation | 2m00' | |
Number of Cycles | 30 | |
Buffer | 5x 10µL | |
MgCl2 | 10µM 0µL | |
dNTP | 10µM 1µL | |
oligoF | 5 DEcoR1-FtsZ-F | 10µM 2.5µL |
oligoR | 2 FtsZ-R | 10µM 2.5µL |
water | 34µL | |
polymerase | Phusion 0.5µL | |
DNA | toughpick in glycerol stock of MG1655 |
PCR : Lox66-DapAColi | ||
---|---|---|
Name | Lox66-DapAColi | |
Annealing T° | 55°C | |
Time of elongation | 2m00' | |
Number of Cycles | 30 | |
Buffer | 5x 10µL | |
MgCl2 | 10µM 0µL | |
dNTP | 10µM 1µL | |
oligoF | 6 Lox66-DapAColi-F | 10µM 2.5µL |
oligoR | 7 DapAColi-R | 10µM 2.5µL |
water | 34µL | |
polymerase | Phusion 0.5µL | |
DNA | toughpick in glycerol stock of MG1655 |