Team:Calgary/23 July 2009
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* No single colonies were found on LB+Kan plates. The transformation was done by using XL Gold Ultracompetent cells and plasmid, pCS26+promoters (NEB Quick Ligase). | * No single colonies were found on LB+Kan plates. The transformation was done by using XL Gold Ultracompetent cells and plasmid, pCS26+promoters (NEB Quick Ligase). | ||
+ | * Transformation of pBluescript into both XL Gold and Top 10 cells were successful. Cells grew on LB plates. | ||
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Revision as of 03:59, 29 July 2009
UNIVERSITY OF CALGARY