Team:Paris/27 July 2009
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==Lab work== | ==Lab work== | ||
- | + | *Media: 15 LB agarosis ampiciline dishes were made. | |
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- | + | *PCR for oligo P1-P2 (tolR); P3-P4 (tolA); P5-P6 (tatABC); P7-P8 (clyA fusion).[[Team:Paris/Protocols_PCRqload | The protocol is stored under the name PCR quick load Taq mix:]]<br> | |
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- | [[Team:Paris/Protocols_PCRqload | | + | |
Revision as of 23:50, 30 July 2009
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NoteBook
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Brain work
edit please ^^
Lab work
- Media: 15 LB agarosis ampiciline dishes were made.
- PCR for oligo P1-P2 (tolR); P3-P4 (tolA); P5-P6 (tatABC); P7-P8 (clyA fusion). The protocol is stored under the name PCR quick load Taq mix:
Preparation for Vf=50µL:
-1µL Matrice
-14µL H2O
-5µ Oligo Fw (à 0,2M)
-5µL Oligo Rw (à 0,2M)
-25µL Tampon+Taq (Taq quick load master mix 2X)
PCR launched with a Tm at 60°C (programme quick load)
- Buffer for Competent bacteria by RbCl
- [F9] Buffer I (250ml)
- [F10] Buffer II (125ml)
- DH5 alpha competent bacteria by RbCl [Protocol]
To do list
migration of the PCR product on a BET gel.