Team:Evry/Notebook/w15

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<h1>Week 15: 17th September - 23rd September</h1>
<h1>Week 15: 17th September - 23rd September</h1>
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<p> this week we have worked to characterize Promotors and Reporters in order to test their validity by injection in tadpoles :
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<li>biobricking promotors in Pcs2+ which are then to be characterized in tadpoles after cloning upstream to various reporters including mCFP, SfGFP, and citrine which are:
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            <ul><li>P Elastase</li>
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                    <li>Hsp70</li>
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                    <li>P Car A</li>
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                    <li> FLk1</li>
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                    <li>P CMV</li></ul>
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this work included standard PCR amplification, purification , plasmid digestion, ligation of vector-insert, transformation, miniprepping, and sequencing.</ul>
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<li>following that  cloning the reporters downstream to various promotors was done </li>
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<li> cloning og IAAh and IAAM in both Psb1C3 and Pcs2+  by standard biobrick portocol </li>
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<li> Golden gate assembly of IAAM-IAAH cassette in both Psb1C3 and Pcs2+ </li>
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<li>Injection in tadpoles for the parts we managed to clone and was validated correctly by sequencing </li>
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Latest revision as of 02:21, 27 September 2012

Weeks:

June July August September October November

Week 15: 17th September - 23rd September

this week we have worked to characterize Promotors and Reporters in order to test their validity by injection in tadpoles :

  • biobricking promotors in Pcs2+ which are then to be characterized in tadpoles after cloning upstream to various reporters including mCFP, SfGFP, and citrine which are:
    • P Elastase
    • Hsp70
    • P Car A
    • FLk1
    • P CMV
    this work included standard PCR amplification, purification , plasmid digestion, ligation of vector-insert, transformation, miniprepping, and sequencing.
  • following that cloning the reporters downstream to various promotors was done
  • cloning og IAAh and IAAM in both Psb1C3 and Pcs2+ by standard biobrick portocol
  • Golden gate assembly of IAAM-IAAH cassette in both Psb1C3 and Pcs2+
  • Injection in tadpoles for the parts we managed to clone and was validated correctly by sequencing