Team:Freiburg/Notebook/10 September

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commons

testdigest

Investigators:Julia

green light receptor

ligation for cloning PcpcG infront of CFP/YFP

Ligation

1. add H2O 11 μl

2. add 2 μl Ligase Buffer 10x

3. add Insert 1

4. add Vector (20ng needed. When proceeding from 3A digestion use 2 μl)

5. Add 1 μl T4-DNA Ligase

6. Incubate 30 min at room temperature

7. heat for 20 minutes at 80°C

blue light receptor

Picking colonies

Investigators:Sophie

inoculating cm-LB with clones from the Gibson-♥-NOT-Trafo.

Labelled ♥-NOT-G a,b,c,d,e,f

Transformation

Investigators: Sophie

Transformation with the PR-♥-NOT-Ligation (6 different PR-vectors)

red light receptor

NAME OF YOUR EXPERIMENT

Investigators:NAME

Lysis cassette

M48 in C3 Vector

Investigators:Theo

Part M48 was Minipreped and cut with EcoRI and PstI. pSB1C3 was also PCR amplified on Friday (this was probably the problem for the failed Transformation of the other part-project -see Notebook Sept 9th-) and cut with EcoRI and PstI, ligated with M48 and transformed into competent cells. The colonies were to be picked on Sunday.

Troubleshooting of lysis cassette

Colonies of the transformation done on Friday were picked and inoculated on Amp LB medium

Precipitator

Inoculation with pbd-clones

Investigators: Sophie

I inoculated 200mL Cm-LB with clones containing the plastic binding domain. I want to extract the GFP-pbd protein to be able to make experiments with this protein and get data about the plastic binding performance