green light receptor
Order primers
Investigators: Jakob
- Order new primers for the quickchange of CcaS and CcaR
- I got the sequence from the iGEM-Team Uppsala THX again!
blue light receptor
Transformation
Investigators: Sophie
Transformation of ligated parts:
- LovTAP
- Not-Gate
- T3 vector
stored in incubator at 37°C.
red light receptor
PCR for Cph8
Investigators:Julia
after protocol from Uppsala.
PCR-Mixture for one Reaction:
For a 50 µl reaction use
32,5µl
| H20
|
|
10µl
| 5x Phusion Buffer
|
|
2.5µl
| Primer fw
|
|
2.5µl
| Primer dw
|
|
1µl
| dNTPs
|
|
1µl
| DNA-Template
|
|
0.5 µl
| Phusion (add in the end)
|
|
Primer used:
cph8 Prefix: TTCGAATTCGCGGCCGCTTCTAGATGGCCACCACCGTACAA
cph8 Suffix: CCGCTACTAGTATTATTACCCTTCTTTTGTCATGCCCT
PCR program:
Temp. Time,Nr of cycles
98° 5' 1x
98° 30 10x
65° 30
72° 1'15
98° 30 20x
72° 1'15
72° 7' 1x
4° ∞
Template: Voights plasmid (10x dilution)
Amplicon: 2235 bp
Elongation time Phusion 67,05 sec
Lysis cassette
2A Assembly of the Lysis Cassette (S4+S15)
Investigators:Theo
Since 3A assemly doesn't want to help us, we are going to try a 2A Assembly of S4 with S15.
S4 is cut with SpeI and PstI.
S15 is cut with XbaI and PstI, and is to be run on a gel, cut, isolated, ligated with S4 and finally transformed in competent cells.
After the gel with S15 was run, I noticed there was no band to be seen and our instructor told me it was because I had not used a lot of DNA (500ng).
I am going to repeat this tomorrow.
Precipitator
Ligation
Investigators: Sophie
continue from experiment: Cloning (12.8.11)
Project name: inducible promoter for pbd
Vector: psb1T3
Inserts: IPTG-Promoter,Pbd-GFP
samples stored in Ruediger's box
Transformation
Investigators: Sophie
continue from experiment: Ligation
Project name: inducible promoter for pbd
samples stored in incubator
PCR
Investigators: Rüdiger
PCR of precipitator.
Primer:
Primer:
name
| primer
| primer
|
44
| p44
| p54
|
45
| p45
| p54
|
46
| p46
| p54
|
48
| p48
| p47
|
51
| p51
| p54
|
52
| p52
| p54
|
53
| p53
| p54
|