green light receptor
1. Quickchange
Investigator:Jakob
Name:
Jakob
| Date:
08.08.2011
|
Continue from Experiment:
|
Project Name:
Quickchange CcaR and CcaS
|
PCR-Mixture for one Reaction:
For a 50 µl reaction use
32,5µl
| H20
|
|
10µl
| 5x Phusion Buffer
|
|
2.5µl
| Primer fw
| Primer: P12(CcaR) and P14(CcaS
|
2.5µl
| Primer dw
| Primer: P13(CcaR) and P15(CcaS)
|
1µl
| dNTPs
|
|
1µl
| DNA-Template
| DNA: CcaR and CcaS
|
0.5 µl
| Phusion (add in the end)
|
|
2. Digest with DpnI
- Digest of the quickchange above
3. Transformation
- Transformation from digest above
- Note: I'm such a fool...forget the gel...
blue light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
red light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
Lysis cassette
NAME OF YOUR EXPERIMENT
Investigators:NAME
Precipitator
NAME OF YOUR EXPERIMENT: Cloning
Investigators: Sophie
continue from experiment: miniprep (the, 8.8.)
Project name: new 3A assembly with amp vector
Parts: psB1A3 (Eco & Pst)
GFP-pbd ( Xba & Pst)
PR4 or PR6 (Eco & Spe)
Why? The last cloning of Theo and Jakob produced one clone with GFP-pbd inside but without PR. So I'm trying again to clone with two different PRs with different RBS strenghts.
Stored in: "Minipreps, verdaut"-box