Team:Calgary/6 July 2009
From 2009.igem.org
(Difference between revisions)
Emily Hicks (Talk | contribs) |
Emily Hicks (Talk | contribs) |
||
Line 216: | Line 216: | ||
Now that we have our gene of interest, LuxOD47E, Biobricked, we can start constuction to add the J13002 promoter and the B0015 terminator. We'll do two constrcutions in parallel and see if one of them works. | Now that we have our gene of interest, LuxOD47E, Biobricked, we can start constuction to add the J13002 promoter and the B0015 terminator. We'll do two constrcutions in parallel and see if one of them works. | ||
- | *Did a restriction digest cutting the insert with EcoRI and SpeI and cutting the recipient with EcoRI and XbaI restriction enzymes. | + | * Did a restriction digest cutting the insert with EcoRI and SpeI and cutting the recipient with EcoRI and XbaI restriction enzymes. |
- | *Performed Antarctic Phosphotase Treatment (NEB) on the recipients, followed by ligation of the inserts and recipients. | + | * Performed Antarctic Phosphotase Treatment (NEB) on the recipients, followed by ligation of the inserts and recipients. |
<html> | <html> | ||
</div> | </div> |
Revision as of 22:49, 17 August 2009
UNIVERSITY OF CALGARY