Team:Paris/27 July 2009
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*PCR for oligo P1-P2 (tolR); P3-P4 (tolA); P5-P6 (tatABC); P7-P8 (clyA fusion). | *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. [[ | + | **Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan. [[Team:Paris/ProtocolsMB#PCR with Quick load Taq2x Master Mix|PCR Quick load protocol]] |
**PCR launched with a Tm at 60°C (programme quick load). | **PCR launched with a Tm at 60°C (programme quick load). | ||
<br> | <br> |
Revision as of 13:13, 10 August 2009
NoteBook
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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. PCR Quick load protocol
- PCR launched with a Tm at 60°C (programme quick load).
- Buffer for Competent bacteria by RbCl
- Buffer I (250ml)
- Buffer II (125ml)
- DH5 alpha competent bacteria by RbCl [Protocol]