Team:Calgary/24 June 2009
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*PCR Products were visualized on a 1% agarose gel run at 120 V with 1.0 KB GeneRuler DNA Ladder. See gel photo below. | *PCR Products were visualized on a 1% agarose gel run at 120 V with 1.0 KB GeneRuler DNA Ladder. See gel photo below. | ||
*Lanes 1-12 contain LuxOD47E in pCR2.1-TOPO vector. Lane 13 is a negative control with only Mastermix + ddH2O. | *Lanes 1-12 contain LuxOD47E in pCR2.1-TOPO vector. Lane 13 is a negative control with only Mastermix + ddH2O. | ||
+ | <Br> | ||
+ | [[Image:2009.06.25BBKAmpPCR.jpg|350px]] | ||
*From this gel, it looks like our gene if interest, LuxOD47E is there as we see bads around 1.4 KB, as expected (gene is 1362 base pairs). We will proceed by isoltaing plasmid from the PCR product and performing a NotI Verification digest. | *From this gel, it looks like our gene if interest, LuxOD47E is there as we see bads around 1.4 KB, as expected (gene is 1362 base pairs). We will proceed by isoltaing plasmid from the PCR product and performing a NotI Verification digest. | ||
*So I pooled the DNA from the BBK amplification PCR. Lanes: 2,3,9,11 and 12 went into tube 1 and lanes 4,5,6,7 and 8 went into tube 2. I did a PCR product isolation (Sigma) according to the manufacturer's instructions and took the concentration using the Nanodrop Spectrophotometer. | *So I pooled the DNA from the BBK amplification PCR. Lanes: 2,3,9,11 and 12 went into tube 1 and lanes 4,5,6,7 and 8 went into tube 2. I did a PCR product isolation (Sigma) according to the manufacturer's instructions and took the concentration using the Nanodrop Spectrophotometer. |
Revision as of 22:56, 13 September 2009
UNIVERSITY OF CALGARY