Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/16

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==2010/08/16 Monday(NEX)==
==2010/08/16 Monday(NEX)==
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===Experiment:Agarose Gel Electro-phoresis===
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===Experiment:Agarose gel Electrophoresis===
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'''Member'''<br />
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:'''Member'''<br />
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NEX and watachin
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:NEX and watachin
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'''Materials'''<br />
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:'''Materials'''<br />
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*PCR production
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:*bcsA,B,C(digestion had been done last Friday)
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*Agarose Gel
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:*1% Agarose Gel
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*10×Loading buffer 5μl
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:*10×Loading buffer
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'''Procedure'''
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:'''Procedure'''
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#Pour the Agarose gel onto gel plate and make wells on it.
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:#Pour the Agarose gel onto gel plate and make wells on it.
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#Apply the 10×Loading buffer in the one of wells.
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:#Apply the 10×Loading buffer in the one of wells.
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#Apply the Insert DNA in another well.
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:#Apply the Insert DNA in another well.
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'''Consequence'''<br />
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:'''Consequence'''<br />
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We could see the bcsB.<br/>
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:We could see a band of bcsB.<br/>
[[Image:20100816.jpg]]
[[Image:20100816.jpg]]

Latest revision as of 21:33, 26 October 2010


E.coli Fiber Project Notebook

August 2010
SUNMONTUEWEDTHUFRISAT
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September 2010
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October 2010
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31

2010/08/16 Monday(NEX)

Experiment:Agarose gel Electrophoresis

Member
NEX and watachin
Materials
  • bcsA,B,C(digestion had been done last Friday)
  • 1% Agarose Gel
  • 10×Loading buffer
Procedure
  1. Pour the Agarose gel onto gel plate and make wells on it.
  2. Apply the 10×Loading buffer in the one of wells.
  3. Apply the Insert DNA in another well.
Consequence
We could see a band of bcsB.

20100816.jpg