From 2009.igem.org
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Revision as of 18:00, 28 July 2009
University of Calgary
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CAROL
Verification of amplification of luxCDABE from polymerase chain reaction (PCR)
- Prepared 0.7% Agarose gel
- Used orange G dye
- Ran gel at 90V for 90 minutes
RESULTS:
- 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.
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CHINMOYEE
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EMILY
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FAHD
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IMAN
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JAMIE
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JEREMY
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KATIE
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KEVIN
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MANDY
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PATRICK
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PRIMA
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STEFAN
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VICKI
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