Team:Freiburg/Notebook/22 August

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green light receptor

second quickchange of CcaS

Investigators:Julia

PCR-Mixture for one Reaction:

For a 50 µl reaction use

What program do you use?

After PCR: Digestion with DpnI in order to get of the old plasmids :

5 µl NEB buffer 4

5 µl BSA (10x)

2 µl DpnI

38 µl of PCR Product

Incubation for 1,5h, deactivation at 80°C  for 20 min.

Transformation with 10 µl of the digested PCR product. Cells were plated out on Kanamycin plates( at 23:00 o’clock ).

blue light receptor

Sequencing

Investigators: Sandra

The sequencing showed that the 3A-assembly did not work. We will send the LovTap PCR product to get sequenced. May be the PCR did not work.

PCR

Investigators: Sandra

PCR of Not-Gate.

P 74:

• actgcagcggccgctgctagca

P 24:

• tatgaattcgcggccgcttctag

PCR product was loaded onto a gel. Expected lane: 900bp
PCR worked and we got Not-Gate with NEHI and PstI.

Cloning

Investigators: Sophie

new 3A assembly with Sandra's NOT-gate-PCR-product, our LOV-Tap-pcr-product (both mutated with NEH1 restriction sites) and an amp-vector
The digested samples were loaded to a gel. They showed clear bands in the right size. Only the band of the vector was not intense enough, so the vector has to be digested again.

red light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME

Lysis cassette

NAME OF YOUR EXPERIMENT

Investigators:NAME

Precipitator

Transformation

Investigators: Rüdiger, Sandra

Transformation of:
61 a,b
62 a,b
63 a,b.

Vector:pSB1C3

Incubation over night.

Cloning for GFP-pbd with IPTG-inucible promoter

Investigator: Sophie
as cloning from 18.08.11 did not work I try it again with longer digestion times.

PCR

PCR-Mixture for one Reaction:

For a 50 µl reaction use

What program do you use?

Anneal Gradient from 61-72°c, 15sec.

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?

Investiagators: Rüdiger