Team:Calgary/21 May 2009
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- | + | Verification of amplification of <i>luxCDABE</i> from polymerase chain reaction (PCR) | |
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- | * | + | * Prepared 0.7% Agarose gel |
- | * | + | * Used orange G dye |
- | * | + | * Ran gel at 90V for 90 minutes |
RESULTS: | RESULTS: | ||
[[Image:luxCDABEPCR.png]] | [[Image:luxCDABEPCR.png]] | ||
- | * | + | *From the results, there is contamination in the negative control, but it did amplify the 6KB <i>LUXCDABE</i>. The large bands is a result of loading too much DNA. |
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Revision as of 17:32, 28 July 2009
UNIVERSITY OF CALGARY