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.[[Team:Paris/ | + | **Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan.[[https://2009.igem.org/wiki/Team:Paris/PCR with Quick load Taq2x Master Mix Protocol]]. |
**PCR launched with a Tm at 60°C (programme quick load). | **PCR launched with a Tm at 60°C (programme quick load). | ||
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Revision as of 23:55, 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).
- Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan.[with Quick load Taq2x Master Mix 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.