Team:Paris/27 July 2009
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*Media: 15 LB agarosis ampiciline dishes were made. | *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 | Protocol]] | + | *PCR for oligo P1-P2 (tolR); P3-P4 (tolA); P5-P6 (tatABC); P7-P8 (clyA fusion). |
- | + | **Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan.[[Team:Paris/Protocols_PCRqload | Protocol]]. | |
- | + | **PCR launched with a Tm at 60°C (programme quick load). | |
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*Buffer for Competent bacteria by RbCl | *Buffer for Competent bacteria by RbCl | ||
**[F9] Buffer I (250ml) | **[F9] Buffer I (250ml) |
Revision as of 23:53, 30 July 2009
Contents |
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).
- Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan. Protocol.
- 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.