Team:Freiburg/Notebook/12 August
From 2011.igem.org
Contents |
Meeting
attendants:
Time:
green light receptor
already done:
To-do:
blue light receptor
already done:
To-do:
red light receptor
already done:
To-do:
Lysis cassette
already done:
To-do:
Precipitator
already done:
To-do:
green light receptor
NAME OF YOUR EXPERIMENT
Investigators:NAME
blue light receptor
Gel of the PCR product: LovTAP
Investigators: Sandra
To confrim the PCR worked this time, we loaded the sample onto a gel. The size of the fragment should be 3000bp.
red light receptor
Picking clones of pcyA and ho1
Investigators: Sandra
Picked 2 clones of each plate:
- 1pTd (PR1+pcyA+terminator)
- 2pTd (PR2+pcyA+terminator)
- 1pTb (PR1+pcyA+terminator)
- 2pTb (PR2+pcyA+terminator)
- 1L23 (PR1+ho1+terminator)
- 2L23 (PR2+ho1+terminator)
Incubation over night.
Lysis cassette
Miniprep
Investigators: Jakob, Ruediger, Theo
Name: Jakob, Ruediger, Theo | Date: 12.08.2011 |
Continue from Experiment: Transformation, 10.08.2011 | |
Project Name:
Lysis systeme, plasticbinding, GST-Tag, IPTG inducible promotor, LOV-Tap |
Documentation:
Why are you doing this experiment? Name the parts which you extract.
- Need the DNA concentration
Describe your results and mistakes and measure the DNA concentration with the Nanodrop and note the results. How did you label your probes and where are they stored?
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Precipitator
NAME OF YOUR EXPERIMENT
Investigators: NAME