Team:Freiburg/Notebook/12 August

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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 1000bp. The gel showed a band at 1000bp. We digested the PCR product with DpnI and then purified the DNA with the PCR purification kit.

3A-assembly of Not-Gate, LovTAP in pSB1T3

Investigators: Sandra

Digestion

Amount of DNA and H20:

Enzymes necessary for digestion:

• Incubation at 37°C for 6 hours
• 20 minutes at 80°C

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

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?

Precipitator

NAME OF YOUR EXPERIMENT

Investigators: NAME