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Team:Freiburg/Notebook/11 August
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Revision as of 13:05, 13 September 2011
Contact 
Contents |
green light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
blue light receptor
PCR
| Name: Sophie
| Date: 11.8.11 |
| Continue from Experiment: new experiment
| |
| Project Name: changes in the LovTAP for 3A assembly | |
PCR-Mixture for one Reaction:
For a 50 µl reaction use
| 32,5µl | H20 | Name |
| 10µl | 5x Phusion Buffer | of Primer |
| 2.5µl | Primer fw | |
| 2.5µl | Primer dw | |
| 1µl | dNTPs | of Template DNA |
| 1µl | DNA-Template | |
| 0.5 µl | Phusion (add in the end) |
What program do you use? Normal PCR with 60°C annealing temperature
To confirm the PCR-Product has the correct size, load 2 µl of the sample onto an agarose-gel.
How did you label the PCR-Product, where is it stored and what do you do next?
red light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
Lysis cassette
NAME OF YOUR EXPERIMENT
Investigators:NAME
Precipitator
Tramsformation with inducible Promoter
Investigators: Sophie We didn't get any clones with both Plastic binding domain and Promoter-RBS inside, the Pbd seems to be toxic when expressed.So we want to try if it is possible to get cells with an inducible Promoter and Pbd. In this case we could cultivate the cells and induce expression of the Pbd only shortly before lysis. As our Light-inducible Promoters are not finished we use the IPTG inducible Promoter BBa_J04500 (Plate4, 12A)
PCR
Investigators: Rüdiger
PCR of precipitator.
Primer fw:
- p51
- p52
- p53
Primer dw:
- p54
DNA template: S43
DMSO was used to reduce Tm about 5°C.
