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Team:Evry/Notebook/June/29
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Latest revision as of 08:57, 9 July 2012
Promoters & Reporters workgroup
Gel preparation
25mL agarose+TAE (frigo) + 2microL BET
Sample preparation
DNA Ladder 1kB: 1microL ladder + 1microL loading buffer + 4microL ddH2O
Digested RFP, YFP, CFP, GFP, pCS2+ (from 28 june) : 10microL sample + 2microL loading buffer
=> 100V, 1h
Result:no DNA detectable, Solution: to redo the step of digestion with more DNA
DNA digestion under construction
4ul of CFP, GFP, RFP, YFP dosed on 28 june
3ul of pSC2+ dosed on 28 june
Gel migration
Gel preparation
50mL agarose+TAE (frigo) + 4ul BET
Sample preparation
DNA Ladder 1kB: 1ul ladder + 1ul loading buffer + 4ul ddH2O
Digested RFP, YFP, CFP, GFP, pCS2+ (from 29 june) : 15ul sample + 3ul loading buffer
=> 100V, 1h
Result: no RFP detectable
Gel extraction under construction
Ligation under construction
