Team:Paris Saclay/Notebook/July/4
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- | We obtain fragment at the right size in wells : 3, 4 , 8 , 9 12 and 13. | + | We obtain fragment at the right size in wells : 3, 4 , 8 , 9 12 and 13. We will digest our biobrick to confirm that Pfnr insert PSB1C3 correctly. |
- | We will | + | |
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Protocol : [[Team:Paris_Saclay/extraction|Hight copy plamid extraction]] | Protocol : [[Team:Paris_Saclay/extraction|Hight copy plamid extraction]] | ||
- | ===='''5 - Digestion of Bba_K1155000 by NotI, MluI, HpaI'''==== | + | ===='''5 - Digestion of Bba_K1155000 by NotI, MluI, HpaI to check good insertion of Pfnr in PSB1C3'''==== |
Abdou | Abdou |
Revision as of 22:44, 23 September 2013
Notebook : July 4
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining Bba_K1155000
1 - Estimation of Pfnr Colony PCR size fragments
Abdou, Anaïs, Sheng
We used software gene manager to find the correct size of our fragments.
Estimated size :
- VF/VR primer -> Plasmid without Pfnr size : 277bp
- VF/Pfnr_down -> Plasmid with Pfnr size : 276bp
- Pfnr_Up/VR -> Plasmid with Pfnr size : 311bp
2 - Electrophoresis of Colony PCR products
Zhou
We obtain fragment at the right size in wells : 3, 4 , 8 , 9 12 and 13. We will digest our biobrick to confirm that Pfnr insert PSB1C3 correctly. |
3 - Stock of Bba_K1155000
Zhou
Used quantities :
- Bba_K1155000 confirmed : 1 mL
- Glycerol : 500µL glycerol.
We stocked them at -20°C.
4 - Extraction of Bba_K1155000 from DH5α
Anaïs, Sheng
Protocol : Hight copy plamid extraction
5 - Digestion of Bba_K1155000 by NotI, MluI, HpaI to check good insertion of Pfnr in PSB1C3
Abdou
Used quantities :
- Bba_K1155000 : 2µL
- Bufer oranger : 2µL
- NotI or MluI or HpaI : 0.5µL
- H2O : 15.5µL
We let the digestion 1h30 at 37°C.
6 - Culture of Bba_K1155000
Anaïs, Sheng
We made 2 cultures of bacterias transformed with Bba_K1155000 that show a fragments at the right size at electrophoresis.
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