Team:Newcastle/Labwork/14 September 2009

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==Metal Sensing team==
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===Introduction===
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===Practical Outline===
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Today's lab session will continue straight on from yesterday's session and fulfil the following objectives:
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<br>
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* Run products of PCR reaction involving the arsR BioBrick (BBa_J33206 in pSB1A2 missing promoter) and cadA promoter region
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** If successful clean up product, run on agarose gel through electrophoresis, excise band and carry out gel extraction.
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** Cut cleaned and excised fragment with BamHI and NheI
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** Carry out ligation (possibly an overnight ligation)
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* Cut pMUTIN4 and cotC (i.e. PCR product 3) with BamHI and HindIII
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** Ligate the fragments (possibly overnight)
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<br>
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===Procedure===
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Revision as of 14:52, 5 October 2009


Lab Work - 14/09/09

Metal Sensing team

Introduction

Practical Outline

Today's lab session will continue straight on from yesterday's session and fulfil the following objectives:

  • Run products of PCR reaction involving the arsR BioBrick (BBa_J33206 in pSB1A2 missing promoter) and cadA promoter region
    • If successful clean up product, run on agarose gel through electrophoresis, excise band and carry out gel extraction.
    • Cut cleaned and excised fragment with BamHI and NheI
    • Carry out ligation (possibly an overnight ligation)
  • Cut pMUTIN4 and cotC (i.e. PCR product 3) with BamHI and HindIII
    • Ligate the fragments (possibly overnight)


Procedure




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