Team:Freiburg/Notebook/23 August
From 2011.igem.org
Contents |
green light receptor
PCR
Investigator: Jakob
PCR
Name:
Jakob | Date:
16.08.2011 |
Continue from Experiment: 12.08.2011
Order primers | |
Project Name:
Quickchange of CcaR (EcoRI) |
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 | P 77 (1:10) |
2.5µl | Primer dw | P 78 (1:10) |
1µl | dNTPs | of Template DNA |
1µl | DNA-Template | CcaR from synechocystis 5ng/µl |
0.5 µl | Phusion (add in the end) |
The program we used: for Quickchange of CcaR (EcoRI)
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blue light receptor
Gel purification
Investigators:Sophie the bands of LOV-pcr and NOT-pcr where purificated. The vector was digested again because the band on the gel was not intense enough.
Ligation
Investigators: Sophie: LOV-pcr, NOT-pcr and the Amp vector where ligated at 16°C
Ligation
Investigators: Sophie I ligated the purified inserts to the vector in the ratio 5:2 and 10:5 because of the loss of DNA due to the gelextraction
Transformation
Investigators: Sophie: Transformation with the ligation product
red light receptor
PCR
Investigator: Jakob
PCR
Name:
Jakob | Date:
16.08.2011 |
Continue from Experiment: 12.08.2011
Order primers | |
Project Name:
Red light receptor, amplify Cph8 |
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 | P 58 (1:10) |
2.5µl | Primer dw | P 59 (1:10) |
1µl | dNTPs | of Template DNA |
1µl | DNA-Template | JT122 5ng/µl |
0.5 µl | Phusion (add in the end) |
The program we used: for Cph8
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Lysis cassette
NAME OF YOUR EXPERIMENT
Investigators:NAME
Precipitator
NAME OF YOUR EXPERIMENT
Investigators: NAME