Team:University of Ottawa/27 May 2008

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==Today in the Lab==
==Today in the Lab==
Matt, Dan, Jon
Matt, Dan, Jon
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<li>Tripel Digestion completed for the first plasmid.  
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::<li>Tripel Digestion completed for the first plasmid.  
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<li>EcorI, PstI and EagI used as the restrction enzymes.
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::<li>EcorI, PstI and EagI used as the restrction enzymes.
-
<li>Gel agarose made for the first plasmid, electrophoresis performed successfully.
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::<li>Gel agarose made for the first plasmid, electrophoresis performed successfully.
-
<li>Gel results were as expected when compared with Nebcutter Gel for the first plasmid.
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::<li>Gel results were as expected when compared with Nebcutter Gel for the first plasmid.
-
<li>Double digestion completed for the second plasmid.  
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::<li>Double digestion completed for the second plasmid.  
-
<li>SacI and NcoI were used as the restrcition enzymes.
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::<li>SacI and NcoI were used as the restrcition enzymes.

Latest revision as of 20:25, 24 July 2008

Untitled Document

 

 


Contents



Today in the Lab

Matt, Dan, Jon

  • Tripel Digestion completed for the first plasmid.
  • EcorI, PstI and EagI used as the restrction enzymes.
  • Gel agarose made for the first plasmid, electrophoresis performed successfully.
  • Gel results were as expected when compared with Nebcutter Gel for the first plasmid.
  • Double digestion completed for the second plasmid.
  • SacI and NcoI were used as the restrcition enzymes.
    • Retrieved from "http://2008.igem.org/Team:University_of_Ottawa/27_May_2008"