Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/17
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(New page: {{:Team:Tokyo_Metropolitan/Header}} ==2010/8/17 Tuesday (watachin)== ===Experiment:Electrophoreses of PCR productions=== '''Member'''<br /> NEX and watachin '''Materials''' *pSB1A3(25ng/...)
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(New page: {{:Team:Tokyo_Metropolitan/Header}} ==2010/8/17 Tuesday (watachin)== ===Experiment:Electrophoreses of PCR productions=== '''Member'''<br /> NEX and watachin '''Materials''' *pSB1A3(25ng/...)
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Revision as of 09:59, 29 August 2010
2010/8/17 Tuesday (watachin)
Experiment:Electrophoreses of PCR productions
Member
NEX and watachin
Materials
- 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 gel box.
- mix Loading Buffer and pSB1C3 and then put in well them(marker sets another well).
- load DNA at 100V for two third of entire (about 15 minutes).
- image the consequence of electrophoreses.
Resalt