Team:Calgary/Notebook/Protocols/nucleaseassay
From 2012.igem.org
(Difference between revisions)
Line 9: | Line 9: | ||
<li>At each timepoint aliquots were taken out of the reaction tubes and run on a 1% gel for 40 minutes and imaged. | <li>At each timepoint aliquots were taken out of the reaction tubes and run on a 1% gel for 40 minutes and imaged. | ||
</ol> | </ol> | ||
- | <br><br><br><br><br><br><br><br> | + | <br><br><br><br><br><br><br><br><br><br><br> |
</html>}} | </html>}} |
Revision as of 03:32, 2 October 2012
Hello! iGEM Calgary's wiki functions best with Javascript enabled, especially for mobile devices. We recommend that you enable Javascript on your device for the best wiki-viewing experience. Thanks!
Nuclease assay
- E. coli genome was prepared using MP bio kit and the DNA was quantified using picogreen assay
- 2µg of DNA was put into each test condition.
- Appropriate buffer(s) were added for each enzyme/enzyme combination in the tubes.
- 10 units of enzyme was added into appropriate conditions
- At each timepoint aliquots were taken out of the reaction tubes and run on a 1% gel for 40 minutes and imaged.