Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/17
From 2010.igem.org
(Difference between revisions)
Line 8: | Line 8: | ||
:'''Material''' | :'''Material''' | ||
:*pSB1A3(25ng/μl) 22μl | :*pSB1A3(25ng/μl) 22μl | ||
- | :* | + | :*10×Loading buffer 2.2μl |
:*DNA Marker 5μl | :*DNA Marker 5μl | ||
- | :* | + | :*1×TAE buffer |
:*1% agarose gel | :*1% agarose gel | ||
Latest revision as of 21:38, 26 October 2010
E.coli Fiber Project Notebook
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2010/8/17 Tuesday (watachin)
Experiment:Electrophoresis
- Member
- NEX and watachin
- Material
- pSB1A3(25ng/μl) 22μl
- 10×Loading buffer 2.2μl
- DNA Marker 5μl
- 1×TAE buffer
- 1% agarose gel
- Procedure
- Set agarose gel and add TAE buffer in electrophoresis tank.
- Mix Loading Buffer and pSB1C3 ,then put them in well (marker sets another well).
- Load DNA at 100V for two thirds of total volume (about 15 minutes).
- Image the consequence of electrophoresis.
- Result
- failure
- Plasmid concentration was too low.
Experiment:Transformation of pSB1A3
- Member
- NEX and watachin
- Material
- pSB1A3 1μl
- competent cell (DH5α) 50μl
- LB + amp plate
- Procedure
- mix pSB1A3 and DH5α
- on ice (30min)
- heat shock 42℃ (45sec)
- on ice (2min)
- inoculate onto plate
- incubate cells at 37℃