Team:Paris/27 July 2009
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==NoteBook== | ==NoteBook== | ||
- | + | {{Paris2009_Calendar}} | |
- | { | + | {{Paris2009_Calendar_Link|26_July_2009|28_July_2009}} |
- | + | <center> '''July 27th''' </center> | |
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<html> | <html> | ||
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</html> | </html> | ||
+ | ===Lab work=== | ||
- | = | + | *Media: 15 LB agarosis ampiciline dishes were made. |
- | + | <br> | |
- | + | <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). | ||
+ | <br> | ||
+ | *Buffer for Competent bacteria by RbCl | ||
+ | **Buffer I (250ml) | ||
+ | **Buffer II (125ml) | ||
+ | *DH5 alpha competent bacteria by [[team:Paris/Protocols_Culture#RbCl|RbCl]] | ||
<html> | <html> | ||
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</html> | </html> | ||
+ | ===To do list=== | ||
- | + | 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