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Team:Tokyo Metropolitan/Notebook/Fiber/2010/10/06
From 2010.igem.org
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| - | *mix 2µl | + | *mix 2µl DNA solution with 2μl TE buffer |
| - | * | + | *apply DNA solution and TE buffer mixture to absorption spectrometer |
*measure DNA density | *measure DNA density | ||
Revision as of 03:59, 13 October 2010
Contents |
2010/10/06 Wednesday (Naoto)
Experiment:Electrophoresis of insert check PCR
member
naoto
material
- insert check PCR production(PCR at 10/05)
If you want to know other materials,see protocol4
procedure
see protocol4
result
All of bands seemed to be vector self ligation
Experiment:PCR of T7promoter~bcsABCD(A.xylinum),T7promoter~bcsEFG(E.coli),RBS~T7polymerase
member
naoto
material
- A colony of A.xylinum
- bcsEFG(E.coli)
- T7 polymerase(BBa_K145001)
If you want to know other materials,see protocol3
procedure
see protocol3
Experiment:Measure DNA density
member
naoto
material
- absorption spectrometer
- bcsA,B,C,D(A.xylinum)
- bcsA,B,C,EFG(E.coli)
- pSB1C3
- TE buffer
procedure
- mix 2µl DNA solution with 2μl TE buffer
- apply DNA solution and TE buffer mixture to absorption spectrometer
- measure DNA density
