Team:Paris Saclay/Notebook/August/2
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(→Objective : obtaining FNR and BphR2 proteins) |
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====''' - Transformation the Gibson assembly mix (August 1st)'''==== | ====''' - Transformation the Gibson assembly mix (August 1st)'''==== | ||
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plasmid pSB1C3 containing BphR2 | plasmid pSB1C3 containing BphR2 | ||
plasmid pSB1C3 containingFNR | plasmid pSB1C3 containingFNR | ||
plasmid pSB1C3 containing RBS-FNR | plasmid pSB1C3 containing RBS-FNR | ||
- | in DH5α | + | in DH5α |
Revision as of 17:19, 3 October 2013
Notebook : August 2
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining BBa_K1155003
1 - Extraction of BBa_K1155003 from DH5α
Damir, Nadia
Tranformation from 07/30/13 works. We will extract plasmid BBa_K1155003. |
Protocol : High-copy plasmid extraction
We extracted plasmid from colony 9, 11 and 12. We eluted our extracted plasmid in 50µL H2O.
2 - Electrophoresis to check the extraction of BBa_K1155003
Damir, Nadia
Expected sizes :
- BBa_K1155003 : 2734 pb
Estimated concentrations :
- Clone 9 : 18ng/µL
- Clone 11 :18ng/µL
- Clone 12 : 18ng/µL
We obtained fragments at the right size (Clone 12 starts 5 min after the others). The extraction was good. We will digest it. |
Objective : obtaining BBa_K1155007
1 - Digestion of BBa_I732017 by EcoRI/SpeI to check sizes of fragments
Damir, Nadia
Used quantities :
- BBa_I732017 : 41µL
- Buffer FD : 5µL
- EcoRI : 2µL
- SpeI : 2µL
We let the digestion at 1h30 at 37°C.
2 -Electrophoresis to check the digestion of BBa_I732017 by EcoRI/SpeI
Damir, Nadia
|
Expected sizes :
- RBS-LacZ : 3093 bp
- pSB1A2 : 2079 bp
We didn't obtain fragments at the right size. We will digest BBa_KI732017 again. |
A - Aerobic/Anaerobic regulation system / B - PCB sensor system
Objective : obtaining FNR and BphR2 proteins
XiaoJing
- Transformation the Gibson assembly mix (August 1st)
plasmid pSB1C3 containing BphR2 plasmid pSB1C3 containingFNR plasmid pSB1C3 containing RBS-FNR in DH5α
Protocol : Bacterial transformation
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