Team:Paris/27 July 2009
From 2009.igem.org
(Difference between revisions)
(→Lab work) |
(→Lab work) |
||
Line 18: | Line 18: | ||
*Media: 15 LB agarosis ampiciline dishes were made. | *Media: 15 LB agarosis ampiciline dishes were made. | ||
<br> | <br> | ||
- | <span/ id=" | + | <span/ id="PCR"> |
*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. [[https://2009.igem.org/Team:Paris/Protocols_PCRqload#PCR_with_Quick_load_Taq2x_Master_Mix Protocol]]. | **Matrice is Genomic DNA of [S2] K12 1655 ΔrecA::Kan. [[https://2009.igem.org/Team:Paris/Protocols_PCRqload#PCR_with_Quick_load_Taq2x_Master_Mix Protocol]]. |
Revision as of 13:08, 9 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. [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]