Team:University of Ottawa/27 May 2008

From 2008.igem.org

(Difference between revisions)
(→Today in the Lab)
(→Today in the Lab)
Line 3: Line 3:
==Today in the Lab==
==Today in the Lab==
Matt, Dan, Jon
Matt, Dan, Jon
-
<li>Tripel Digestion completed for the first plasmid.
+
<li>Tripel Digestion completed for the first plasmid.
 +
<li>EcorI, PstI and EagI used as the restrction enzymes.
<li>Gel agarose made for the first plasmid, electrophoresis performed successfully.
<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.
<li>Gel results were as expected when compared with Nebcutter Gel for the first plasmid.
-
<li>Tripel digestion completed for the second plasmid.
+
<li>Double digestion completed for the second plasmid.
 +
<li>SacI and NcoI were used as the restrcition enzymes.

Revision as of 19:24, 27 May 2008

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"