green light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
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
PCR
Name:
Ruediger
| Date:
18.07.2011
|
Continue from Experiment (Date)PCR 1507
(Name) Ruediger
|
Project Name:
GFP Pbd
|
PCR-Mixture for one Reaction:
For a 50 µl reaction use
32,5µl
| H20
|
|
10µl
| 5x Phusion Buffer
|
|
2.5µl
| Primer fw
|
|
2.5µl
| Primer dw
|
|
1µl
| dNTPs
|
|
1µl
| DNA-Template
|
|
0.5 µl
| Phusion (add in the end)
|
|
What program do you use?
10x (95C-41C/47C/52C-72C) + 25x ((95C-60C-72C)
How did you label the PCR-Product, where is it stored and what do you do next?
Reactions:
P28+P18+M14.1
P28+P19+M14.1
P28+P20+M14.1
P28+P2+M14.1
P28+P3+M14.1
P1+P18+M14.1
P1+P19+M14.1
P1+P20+M14.1
P1+P2+M14.1
P1+P3+M14.1
P1+P3+M14.2
Upper panel:All lanes at 41C
Lane 1
| Lane 2
| Lane 3
| Lane 4
| Lane 5
| Lane 6
| Lane 7
| Lane 8
| Lane 9
| Lane 10
|
Quick Load Marker
| P28+P18+M14.1
| P28+P19+M14.1
| P28+P20+M14.1
| P28+P2+M14.1
|
| P1+P19+M14.1
|
| P1+P20+M14.1
| P1+P2+M14.1
|
Lower Panel
Lane 1
| Lane 2
| Lane 3
| Lane 4
| Lane 5
| Lane 6
| Lane 7
| Lane 8
| Lane 9
| Lane 10
|
Quick Load Marker
| P1+P3+M14.1
41C
| P1+P3+M14.1
47C
| P1+P3+M14.2
52C
| P1+P3+M14.1
52C
| P28+P3+M14.1
41C
| P1+P18+M14.1
41C
| P28+P3+M14.1
47C
| P28+P3+M14.1
52C
|
|
Upper Panel: all at 47C
Lane 1
| Lane 2
| Lane 3
| Lane 4
| Lane 5
| Lane 6
| Lane 7
| Lane 8
| Lane 9
| Lane 10
|
Quick Load Marker
| P28+P18+M14.1
| P28+P19+M14.1
| P28+P20+M14.1
| P28+P2+M14.1
|
| P1+P18+M14.1
| P1+P19+M14.1
| P1+P20+M14.1
| P1+P2+M14.1
|
Lower Panel: all at 52C
Lane 1
| Lane 2
| Lane 3
| Lane 4
| Lane 5
| Lane 6
| Lane 7
| Lane 8
| Lane 9
| Lane 10
|
Quick Load Marker
| P28+P18+M14.1
| P28+P19+M14.1
| P28+P20+M14.1
| P28+P2+M14.1
|
| P1+P18+M14.1
| P1+P19+M14.1
| P1+P20+M14.1
| P1+P2+M14.1
|