Paris/July 16
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+ | == Transformations of Biobricks == |
Revision as of 07:59, 17 July 2007
Contents |
Plasmid pKs::DGAT expression in E. Coli
We tried to see TG with NR died on E. Coli cells transfected with pKs::DGAT, an IPTG-inducible promoter.
We tried different growth media containing more or less oleate, that should in theory increase TG synthesis.
Results : we don't see the inductible effect of IPTG. We can think that :
- Either the fluorescence without IPTG is due to a leak of the promoter
- Either DGAT is not induce in presence of IPTG, and the fluorescence we see is only a background.
Growth kinetics of w121 strain
Results of the previous day : we lost everything because of a crash of the computer :( Sorry Eimad !
Transduction of MG1655 with P1 stock made on w121
- Control (1mL LB MgSO4 30mM; CaCl2 15mM)
- 5µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
- 50µL Phage + 900µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
- 500µL Phage + 500µL LB (MgSO4 30mM; CaCl2 15mM) + 100µL MG1655 Culture ON
=>For the nth time, it is not working : we have only contaminants.
MiniPreps
- I0500 clones 1, 2
- pJ23107 clones 1, 2
PCR purification
- Lox71-FtsZ1
- FtsZ2
- DGAT1
- DGAT2
PCRs
The Lox66-DapAColi PCR did not work... We'll try again with different annealing temperature
Assembly PCRs:
- Lox71-FtsA-FtsZ-1 + FtsZ-2
- DGAT-1 + DGAT-2
The Lox66-DapAColi PCR did not work... so we try a gradient of annealing temperatures
PCR : Lox66-DapAColi | ||
---|---|---|
Name | Lox66-DapAColi | |
Annealing T° | 50-65°C | |
Time of elongation | 2m00' | |
Number of Cycles | 35 | |
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 | toothpick in glycerol stock of MG1655 |