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Team:University of Ottawa/27 May 2008
From 2008.igem.org
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==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>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>Double digestion completed for the second plasmid. | + | ::<li>Double digestion completed for the second plasmid. |
| - | <li>SacI and NcoI were used as the restrcition enzymes. | + | ::<li>SacI and NcoI were used as the restrcition enzymes. |
Latest revision as of 20:25, 24 July 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.
