Team:Paris/27 July 2009
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- | ==Lab work== | + | |
*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/ | + | <span/ id="PCR"> |
- | + | *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/ProtocolsMB#PCR with Quick load Taq2x Master Mix|PCR Quick load 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 | ||
- | ** | + | **Buffer I (250ml) |
- | ** | + | **Buffer II (125ml) |
- | *DH5 alpha competent bacteria by | + | *DH5 alpha competent bacteria by [[team:Paris/Protocols_Culture#RbCl|RbCl]] |
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- | ==To do list== | + | ===To do list=== |
migration of the PCR product on a BET gel. | migration of the PCR product on a BET gel. | ||
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+ | {{Paris2009_Calendar_Link|26_July_2009|28_July_2009}} |
Latest 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