Team:Paris/27 July 2009
From 2009.igem.org
(Difference between revisions)
(→Lab work) |
Christophe.R (Talk | contribs) (→Lab work) |
||
(19 intermediate revisions not shown) | |||
Line 14: | Line 14: | ||
</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> | ||
Line 27: | Line 36: | ||
</html> | </html> | ||
+ | ===To do list=== | ||
- | + | migration of the PCR product on a BET gel. | |
- | |||
- | |||
- | + | {{Paris2009_Calendar_Link|26_July_2009|28_July_2009}} | |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + | ||
- | + |
Latest revision as of 13:13, 10 August 2009
NoteBook
|
|
|
|
|
---|
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