Team:Calgary/22 June 2009
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Prima.moinul (Talk | contribs) |
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*See gel photo below. Lanes 1-6 are LuxOD47E cut with XbaI / PstI, colonies 1-6, Lane 7 is a ngeative control with ddH2O. | *See gel photo below. Lanes 1-6 are LuxOD47E cut with XbaI / PstI, colonies 1-6, Lane 7 is a ngeative control with ddH2O. | ||
*Results: Nothing was amplified. This was because I used the wrong buffer. Will proceed by re-running the Colony PCR with the CORRECT buffer (10x PCR Buffer- Cl2). | *Results: Nothing was amplified. This was because I used the wrong buffer. Will proceed by re-running the Colony PCR with the CORRECT buffer (10x PCR Buffer- Cl2). | ||
+ | *Performed colony PCR again with the proper PCR Buffer this time. PCR products were visualized on a 1% agarose gel run at 120 V with Generuler 1.0 KB+ DNA Ladder. Lanes 1-7 are LuxOD47E in psB1AC3 cut with XbaI / PstI. Lane 8 is a negative control with only Mastermix + ddH2O. | ||
+ | *See gel photo below. | ||
+ | *From this gel, it looks like LuxOD47E is in the vector as we see the approproate band size of approximately 1.4 KB. | ||
+ | *Prepared overnight cultures of the colonies, will isolate plasmid tomorrow. | ||
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Revision as of 14:10, 21 August 2009
UNIVERSITY OF CALGARY