Team:Calgary/31 July 2009
From 2009.igem.org
(Difference between revisions)
Line 384: | Line 384: | ||
</html> | </html> | ||
In order to verify cPCR, I have once again ran a cPCR of the reporter circuit, <i>Pqrr4</i>+B0034(RBS)+K082003(GFP+LVA) with <i>Pqrr4</i> Forward and Biobrick CP Reverse primers. Of course, pTaq was used to amplify the DNA. The product was then ran on 2% agarose gel at 90V. ----the gel is being run right now, will edit--- | In order to verify cPCR, I have once again ran a cPCR of the reporter circuit, <i>Pqrr4</i>+B0034(RBS)+K082003(GFP+LVA) with <i>Pqrr4</i> Forward and Biobrick CP Reverse primers. Of course, pTaq was used to amplify the DNA. The product was then ran on 2% agarose gel at 90V. ----the gel is being run right now, will edit--- | ||
- | <br> | + | <br><br> |
<b>Distribution of our baking sale posters</b><br><br> | <b>Distribution of our baking sale posters</b><br><br> | ||
Fahd left a stack of Baking sale posters for us to post throughout the building, and they were posted before 11am today. | Fahd left a stack of Baking sale posters for us to post throughout the building, and they were posted before 11am today. |
Revision as of 22:23, 31 July 2009
UNIVERSITY OF CALGARY