Team:Calgary/21 May 2009

From 2009.igem.org

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VERIFICATION OF AMPLIFICATION OF <i>LUXCDABE</i> FROM POLYMERASE CHAIN REACTION (PCR)
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Verification of amplification of <i>luxCDABE</i> from polymerase chain reaction (PCR)
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* PREPARED 0.7% AGARROSE GEL
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* Prepared 0.7% Agarose gel
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* USED ORANGE G DYE
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* Used orange G dye
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* RAN GEL AT 90V FOR 90 MINUTES
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* Ran gel at 90V for 90 minutes
RESULTS:
RESULTS:
[[Image:luxCDABEPCR.png]]
[[Image:luxCDABEPCR.png]]
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*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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*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

UNIVERSITY OF CALGARY



NOTEBOOK PAGE INDEX


JULY 23, 2009 (DATE)


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: LuxCDABEPCR.png

  • 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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