Commons
PCR
| Name: Sophie
| Date: 17.08.11
|
| Continue from Experiment (Date)
(Name): Commons
|
| Project Name: tet-vector seems to make problems, so a new PCR with original DNA is made
|
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
| SB-prep-3P-1
|
| 2.5µl
| Primer dw
| SB-prep-2Ea
|
| 1µl
| dNTPs
| of Template DNA
|
| 1µl
| DNA-Template
|
PSB 1 T3
|
| 0.5 µl
| Phusion (add in the end)
|
|
What program do you use?
- 2Min 94°C
- 30s 94°C
- 30s 55°C
- 3min 72°C
- 10min 72°C
step 2,3 and 4 in 35 cycles
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?
Labeled PSB 1 T3 stored in -20°C in last drawer
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
Investigators: NAME
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