"
Team:uOttawa CA/Results
From 2012.igem.org
(Difference between revisions)
| Line 4: | Line 4: | ||
<table class="center bold" width="970"> | <table class="center bold" width="970"> | ||
<tr> | <tr> | ||
| - | <td><a href="#scroll-one" class="Orange"> | + | <td><a href="#scroll-one" class="Orange">Characterization data</a></td> |
| - | <td><a href="#scroll-two" class="Orange"> | + | <td><a href="#scroll-two" class="Orange">Promoter Results</a></td> |
| - | <td><a href="#scroll-three" class="Orange"> | + | <td><a href="#scroll-three" class="Orange">Protocols</a></td> |
</tr> | </tr> | ||
</table><br /><br /> | </table><br /><br /> | ||
Revision as of 02:46, 4 October 2012
 |
 |
 |
 |
 |
 |
 |
 |
| Characterization data | Promoter Results | Protocols |
Characterization Data
The strains for characterizing the Tet repressor have been built. Characterization data of the Tet-BFP diploid strains (b) are shown below.
Promoter Design
To test our promoter design protocol, we decided to use the vector PRS416 and primers comprising the distal region of the GAL1 promoter with GAL4 binding sites replaced with tet operator sites. We submitted 9 plasmids for sequencing and our results below elucidate the sequence of our GAL-1 promoter within the PRS416 plasmid:
