Team:Tokyo Metropolitan/Notebook/Fiber/2010/08/17

From 2010.igem.org

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==2010/8/17 Tuesday (watachin)==
==2010/8/17 Tuesday (watachin)==
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===Experiment:Electrophoreses of PCR productions===
+
===Experiment:Electrophoresis===
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'''Member'''<br />
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:'''Member'''
-
NEX and watachin
+
:NEX and watachin
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'''Materials'''
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:'''Material'''
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*pSB1A3(25ng/μl) 22μl
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:*pSB1A3(25ng/μl) 22μl
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*10*Loading buffer 2.2μl  
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:*10×Loading buffer 2.2μl  
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*DNA Marker 5μl
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:*DNA Marker 5μl
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*1*TAE buffer
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:*1×TAE buffer
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*1% agarose gel
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:*1% agarose gel
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'''Procedure'''
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:'''Procedure'''
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#Set agarose gel and add TAE buffer in electrophoresis tank.
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:#Set agarose gel and add TAE buffer in electrophoresis tank.
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#Mix Loading Buffer and pSB1C3 ,then put them in well (marker sets another well).
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:#Mix Loading Buffer and pSB1C3 ,then put them in well (marker sets another well).
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#Load DNA at 100V for two thirds of total volume (about 15 minutes).
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:#Load DNA at 100V for two thirds of total volume (about 15 minutes).
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#Image the consequence of electrophoresis.
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:#Image the consequence of electrophoresis.
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'''Result'''
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:'''Result'''
[[Image:2010-08-17-ef.jpg]]
[[Image:2010-08-17-ef.jpg]]
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failure
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:failure
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Plasmid concentration was too low.
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:Plasmid concentration was too low.
===Experiment:Transformation of pSB1A3===
===Experiment:Transformation of pSB1A3===
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'''Member'''<br />
+
:'''Member'''
-
NEX and watachin
+
:NEX and watachin
-
 
+
-
'''Material'''
+
-
*pSB1A3 1μl
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*competent cell DH5α 50μl
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*LB + amp plate
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+
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'''Procedure'''
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#mix pSB1A3 and DH5α
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#on ice (30min)
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#heat shock 42℃ 45sec
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#on ice (2min)
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#inoculate this onto plate
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#incubate cells at 37℃
+
-
 
+
 +
:'''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℃
<br/>
<br/>

Latest revision as of 21:38, 26 October 2010


E.coli Fiber Project Notebook

August 2010
SUNMONTUEWEDTHUFRISAT
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September 2010
SUNMONTUEWEDTHUFRISAT
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October 2010
SUNMONTUEWEDTHUFRISAT
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31

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
  1. Set agarose gel and add TAE buffer in electrophoresis tank.
  2. Mix Loading Buffer and pSB1C3 ,then put them in well (marker sets another well).
  3. Load DNA at 100V for two thirds of total volume (about 15 minutes).
  4. Image the consequence of electrophoresis.
Result

2010-08-17-ef.jpg

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
  1. mix pSB1A3 and DH5α
  2. on ice (30min)
  3. heat shock 42℃ (45sec)
  4. on ice (2min)
  5. inoculate onto plate
  6. incubate cells at 37℃