Team:Osaka/week3

From 2012.igem.org

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{{Osaka}}
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__NOTOC__
__NOTOC__
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==August 12 (Sun)==
==August 12 (Sun)==
# Miniprep of yesterday's culture
# Miniprep of yesterday's culture
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#* 155(C):1-2D(upstream)+1-23L(downstream)+1-1A(vector)
#* 155(C):1-2D(upstream)+1-23L(downstream)+1-1A(vector)
# SDS-PAGE  
# SDS-PAGE  
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#* Gel electrophoresis
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#* Electrophoresis
==August 16 (Thu)==
==August 16 (Thu)==
# Transformaton of ligation products into DH5α <i>E.coli</i>:153~155
# Transformaton of ligation products into DH5α <i>E.coli</i>:153~155
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# Transformation of plasmid DNA into Rosetta <i>E.coli</i>:empty vector(A)
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# Transformation of plasmid DNA into Rosetta <i>E.coli</i>:151
==August 17 (Fri)==
==August 17 (Fri)==
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==August 18 (Sat)==
==August 18 (Sat)==
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# Preparation of LB agar plates  
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# Preparation of LB agar plates (Tet,Kan)
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# Miniprep of yesterday's culture
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# Miniprep of yesterday's culture:153~155
# PCR
# PCR
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#*mutation was found in PpA → retrial
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#* mutation was found in PprA → retrial
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# Purification of PCR products
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# Preparation of glycerol stock of cell culture:151
# Restriction digests of minipreppped parts
# Restriction digests of minipreppped parts
# Gel electrophoresis of digests  
# Gel electrophoresis of digests  
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# PCR purification
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#* 155 x
# Ligation
# Ligation
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#*  
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#* 156(T):153(upstream)+1-23L(downstream)+1-7A(vector)
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# Transformation of ligation products into DH5α <i>E.coli</i>:155,156
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Latest revision as of 01:30, 14 September 2012


August 12 (Sun)

  1. Miniprep of yesterday's culture
  2. Restriction digests of minipreppped parts
  3. Gel electrophoresis of digests
  4. Ligation
    • 153(C):1-2M(upstream)+1-10H(downstream)+1-1A(vector)
    • 154(C):1-22A(upstream)+1-2M(downstream)+1-1A(vector)
    • 155(C):1-2D(upstream)+1-23L(downstream)+1-1A(vector)
  5. SDS-PAGE
    • Electrophoresis

August 16 (Thu)

  1. Transformaton of ligation products into DH5α E.coli:153~155
  2. Transformation of plasmid DNA into Rosetta E.coli:151

August 17 (Fri)

  1. Transfer to liquid culture

August 18 (Sat)

  1. Preparation of LB agar plates (Tet,Kan)
  2. Miniprep of yesterday's culture:153~155
  3. PCR
    • mutation was found in PprA → retrial
  4. Purification of PCR products
  5. Preparation of glycerol stock of cell culture:151
  6. Restriction digests of minipreppped parts
  7. Gel electrophoresis of digests
    • 155 x
  8. Ligation
    • 156(T):153(upstream)+1-23L(downstream)+1-7A(vector)
  9. Transformation of ligation products into DH5α E.coli:155,156

Back to Notebook