Team:Chiba/Calendar-Home/10 September 2008
From 2008.igem.org
9 September 2008 <|> 11 September 2008
Contents |
Laboratory work
Team:Input
no work
Team:Communication
(9/9)-->Colony Count
- LuxI([http://partsregistry.org/Part:BBa_K084012 BBa_K084012])
- LuxI+LVA([http://partsregistry.org/Part:BBa_K084014 BBa_K084014])
- LasI([http://partsregistry.org/Part:BBa_K084007 BBa_K084007])
- Background([http://partsregistry.org/Part:BBa_R0010 R0010])
- Background([http://partsregistry.org/Part:BBa_C0261 BBa_C0261])
Pick colony
- Colony PCR of 10 colonies from ligation plate(9/9-(2)) and 3 colonies from ligation plate(9/9-(3)) one from control plate([http://partsregistry.org/Part:BBa_F2620 BBa_F2620](2007)).
DNA Template(μL) 1 dNTP mix(μL) 5 Foward Primer(μL) 0.3 Reverse Primer(μL) 0.3 taq DNA polymerase(μL) 0.5 Thermopol Buffer(μL) 3 Nuclease free water(μL) 20 TOTAL(μL) 30
- 95°C,5min -> ( 95°C,1min -> 52°C,1min -> 72°C,1min )・・・25cycles -> 72°C,10min -> 6°C
-->Gel Check
--->(28/8)Miniprepeluted with 50μL of TE buffer.
Team:Output
-->Gel check
-->Mini prep