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
| Name of part
|
insert 1
| 4 μl PcpcG from PCR
|
vector
| 2 μl [http://partsregistry.org/wiki/index.php?title=Part:BBa_I15016 BBa_I15016] /[http://partsregistry.org/wiki/index.php?title=Part:BBa_I15016 BBa_I1501]7
|
H2O
| 11 μl
|
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
NAME OF YOUR EXPERIMENT
Investigators:NAME
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