IGEM:Groningen/Notebook/iGEM 2011/2011/07/22

From OpenWetWare

< IGEM:Groningen | Notebook/iGEM 2011 | 2011 | 07
Revision as of 04:38, 22 July 2011 by Joyce Mulder (Talk | contribs)
(diff) ←Older revision | Current revision (diff) | Newer revision→ (diff)
Jump to: navigation, search
Project name Main project page
Previous entry      Next entry

22-07-11



Plates of transformants with LasR-LVA DT vector look good, since the self ligation plates don't have much colonies!
10μl plate is empty on self ligation plate control! 90μl plate has a few colonies (5)
Colony PCR as usual

Digestion PBAD, PhybB and vectors: cI-LVA and RBS-GFP

PBAD:
15μl PBAD
1μl SpeI
2μl Tango buffer
2μ MQ water

PhybB
3μl PhybB
1μl SpeI
2μl Tango buffer
14μl MQ water

After 1h and 50 minutes: put 2.5μl Tango buffer+ 1μl EcoRI in these samples and digest for another 1h and 50 minm.
DNA clean up with kit of Roche.

Ligation:
PBAD-cI-LVA-DT
6μl PBAD
8.5μl cI-LVA-DT vector
2μl T4 DNA ligase buffer
1μl T4 DNA ligase
2.5μl MQ water

PhybB-cI-LVA-DT
6μl PhybB
8.5μl cI-LVA-DT vector
2μl T4 DNA ligase buffer
1μl T4 DNA ligase
2.5μl MQ water

PBAD-RBS-GFP-DT
6.2μl PhybB
8.5μl cI-LVA-DT vector
2μl T4 DNA ligase buffer
1μl T4 DNA ligase
2.3μl MQ water

Ligate for 30 to 45 minutes

Transformation as usual

Personal tools