Team:Calgary/21 May 2009
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UNIVERSITY OF CALGARY
Verification of amplification of luxCDABE 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
- From the results, there is contamination in the negative control, but it did amplify the 6KB LUXCDABE. The large bands is a result of loading too much DNA.
CHINMOYEE
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EMILY
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FAHD
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IMAN
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PATRICK
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PRIMA
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