Team:HokkaidoU Japan/Notebook/September15

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Transformation using heat shock went well and produced about 100 colonies. We chose 10 and did colony PCR to check if insert was correct. The insert was Arabinose promoter[[http://partsregistry.org/Part:BBa_I0500 (BBa_I0500)]] and GFP reporter[http://partsregistry.org/Part:BBa_E0840 (BBa_E0840)]. Vector used was [http://partsregistry.org/wiki/index.php?title=Part:pSB1C3 pSB1C3].
Transformation using heat shock went well and produced about 100 colonies. We chose 10 and did colony PCR to check if insert was correct. The insert was Arabinose promoter[[http://partsregistry.org/Part:BBa_I0500 (BBa_I0500)]] and GFP reporter[http://partsregistry.org/Part:BBa_E0840 (BBa_E0840)]. Vector used was [http://partsregistry.org/wiki/index.php?title=Part:pSB1C3 pSB1C3].
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Combined length of insert with prefix, suffix and is estimated to be

Revision as of 12:02, 15 September 2010

  • Observed results of yesterdays transformation
    • Transformation using heat shock went well
    • Electroporation transformation failed produce colonies
  • Did Colony PCR of yesterdays transformed colonies
  • Introduced colonies to L(+)Arabinose medium to check if it would show desired function
    • Check for results tomorrow


Result of yesterdays transformation

Transformation using heat shock went well and produced about 100 colonies. We chose 10 and did colony PCR to check if insert was correct. The insert was Arabinose promoterhttp://partsregistry.org/Part:BBa_I0500 (BBa_I0500) and GFP reporter[http://partsregistry.org/Part:BBa_E0840 (BBa_E0840)]. Vector used was [http://partsregistry.org/wiki/index.php?title=Part:pSB1C3 pSB1C3].

Combined length of insert with prefix, suffix and is estimated to be
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