Team:Paris Saclay/Notebook/July/12
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==='''A - Aerobic/Anaerobic regulation system'''=== | ==='''A - Aerobic/Anaerobic regulation system'''=== | ||
- | ===='''Objective : obtaining | + | ===='''Objective : obtaining BBa_K1155003, BBa_K1155007'''==== |
- | ===='''1 -Transformation of | + | ===='''1 -Transformation of BBa_I732019, BBa_B0015, BBa_B0017'''==== |
Zhou | Zhou | ||
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| style="border:1px solid black;padding:5px;background-color:#DE;" | | | style="border:1px solid black;padding:5px;background-color:#DE;" | | ||
- | Transformation of 07/10/13 of | + | Transformation of 07/10/13 of BBa_I732019 didn't works. We will do it again. |
|} | |} | ||
- | Protocol : [[Team:Paris_Saclay/Protocols/ | + | Protocol : [[Team:Paris_Saclay/Protocols/Transformation|Bacterial transformation]] |
===='''2 -Design of RBS-AmilCP oligos'''==== | ===='''2 -Design of RBS-AmilCP oligos'''==== | ||
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We used software gene manager to find the correct oligopeptides for amplification of RBS-Amil CP. | We used software gene manager to find the correct oligopeptides for amplification of RBS-Amil CP. | ||
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==='''B - PCB sensor system'''=== | ==='''B - PCB sensor system'''=== | ||
- | ===='''Objective : obtaining | + | ===='''Objective : obtaining BBa_K1155001, BBa_K1155002 and BphR2'''==== |
- | ===='''1 - Stock of clones 5, 6, 7, 8 for | + | ===='''1 - Stock of clones 5, 6, 7, 8 for BBa_K1155002, clones 5, 6 for BBa_K1155001 and clones 3, 4 for BphR2'''==== |
Zhou | Zhou | ||
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* Culture : 1µL | * Culture : 1µL | ||
- | ===='''2 - Extraction of clones 5, 6, 7, 8 for | + | ===='''2 - Extraction of clones 5, 6, 7, 8 for BBa_K1155002, clones 5, 6 for BBa_K1155001 and clones 3, 4 for BphR2 from DH5α'''==== |
Abdou, Sheng | Abdou, Sheng | ||
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Protocol : [[Team:Paris_Saclay/extraction|High copy plamid extraction]] | Protocol : [[Team:Paris_Saclay/extraction|High copy plamid extraction]] | ||
- | ===='''3 - Streak of | + | ===='''3 - Streak of BBa_K1155002 and BphR2'''==== |
Anaïs | Anaïs | ||
- | We | + | We streak 25 colonies of 07/10/13 transformation of BphA1 and BphR2 in new solid culture. |
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{| border="1" align="center" | {| border="1" align="center" |
Latest revision as of 09:55, 30 September 2013
Notebook : July 12
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining BBa_K1155003, BBa_K1155007
1 -Transformation of BBa_I732019, BBa_B0015, BBa_B0017
Zhou
Transformation of 07/10/13 of BBa_I732019 didn't works. We will do it again. |
Protocol : Bacterial transformation
2 -Design of RBS-AmilCP oligos
Abdou, Anaïs
We used software gene manager to find the correct oligopeptides for amplification of RBS-Amil CP.
B - PCB sensor system
Objective : obtaining BBa_K1155001, BBa_K1155002 and BphR2
1 - Stock of clones 5, 6, 7, 8 for BBa_K1155002, clones 5, 6 for BBa_K1155001 and clones 3, 4 for BphR2
Zhou
Used quantities :
- Glycerol 85% : 425
- Culture : 1µL
2 - Extraction of clones 5, 6, 7, 8 for BBa_K1155002, clones 5, 6 for BBa_K1155001 and clones 3, 4 for BphR2 from DH5α
Abdou, Sheng
Protocol : High copy plamid extraction
3 - Streak of BBa_K1155002 and BphR2
Anaïs
We streak 25 colonies of 07/10/13 transformation of BphA1 and BphR2 in new solid culture.
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