Team:Paris Saclay/Notebook/August/28
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*We got purple clonies on ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3 | *We got purple clonies on ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3 | ||
- | so we do a purify of 4 clonies in two plate. | + | so we do a purify of 4 clonies in two plate.incubated at 37°C in aerobic and anaerobic condition over night to verify the different. |
+ | *Prepare LB plates with Chlorenphenicol and Xgal .Pufify single conle of promoter fnr(activator)nirB plus RBS_LacZ+Term_PSB1C3 and promoter fnr(repressor) plus RBS_LacZ+Term_PSB1C3 to see if color will change. | ||
* Gel extration of Digestion Dnp1 purification of the the PSB1C3 clean for Gibson and do Gibson assembly again . | * Gel extration of Digestion Dnp1 purification of the the PSB1C3 clean for Gibson and do Gibson assembly again . |
Revision as of 15:58, 12 September 2013
Notebook : August 27
summary
- We got purple clonies on ligation promoter fnr(repressor) plus RBS_AmilCP+Term_PSB1C3
so we do a purify of 4 clonies in two plate.incubated at 37°C in aerobic and anaerobic condition over night to verify the different.
- Prepare LB plates with Chlorenphenicol and Xgal .Pufify single conle of promoter fnr(activator)nirB plus RBS_LacZ+Term_PSB1C3 and promoter fnr(repressor) plus RBS_LacZ+Term_PSB1C3 to see if color will change.
- Gel extration of Digestion Dnp1 purification of the the PSB1C3 clean for Gibson and do Gibson assembly again .
lab work
A - Aerobic/Anaerobic regulation system / B - PCB sensing system
- 1 - Gel extraction of the PSB1C3 Clean for Gibson.
Protocol : Gel extraction
- 2- Migration of 3µl PSB1C3 Clean for Gibson (product gel extraction) '
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- 3- product quantification.
- We used the nano drop to measure the DNA in 260nm and we found its concentration
name | PSB1C3 Clean dig Dnp1 gel extraction |
conc. | 37.2ng/µl |
- 4 - Gibson assembly.
- RBS_BphR2_part1, BphR2_part2 and plasmid PSB1C3
- FNR_part1, FNR part1 and plasmid PSB1C3
- RBS_FNR part1, FNR_part2 and plasmid PSB1C3
Sample Volume:
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These 3 mixture is incubated at 50°C for up to one hour. Transformation and spread in 6 LB plates with Chlorenphenicol . Incubate at 37°C over night.
A - Aerobic/Anaerobic regulation system
- 1 - Purify single clone of promoter fnr(activator)nirB + RBS_LacZ+Term_PSB1C3 on plates wiht Chlorenphenicol and Xgal.incubated at 37°C in anaerobic condition over night.
Protocol : Purify single clone
- 2 - Purify single clone of promoter promoter fnr(repressor)+ RBS_LacZ+Term_PSB1C3 on plates wiht Chlorenphenicol and Xgal.incubated at 37°C in aerobic condition over night
- 3 - Purify single clone of promoter fnr(activator)nirB + RBS_AmilCP+Term_PSB1C3 on plates wiht Chlorenphenicol.incubated at 37°C in anaerobic condition over night
- 4 - Purify 4 single purple colony of promoter fnr(repressor)+ RBS_AmilCP+Term_PSB1C3 on two plates wiht Chlorenphenicol .incubated at 37°C in aerobic and anaerobic condition over night
- 5- Purify single clone of B5 promoter fnr(activator)nirB + RBS_AmilCP+Term_PSB1C3 on plates wiht Chlorenphenicol.incubated at 37°C in anaerobic condition over night
- 6- Purify single clone of D1, D5, D6 promoter fnr(repressor)+ RBS_AmilCP+Term_PSB1C3 on two plates wiht Chlorenphenicol .incubated at 37°C in aerobic and anaerobic condition over night
- 7- Purify single clone of C1, C2, C5 ,C6promoter promoter fnr(repressor)+ RBS_LacZ+Term_PSB1C3 on plates wiht Chlorenphenicol and Xgal.incubated at 37°C in aerobic condition over night
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