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Team:WashU/Notebook/Transformation
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Additional, this team transformed plasmids into e. coli in order to amplify plasmids for use by the other teams. This procedure consisted of transforming the plasmid into the bacterial genome, culturing the transformed bacteria, and isolating the DNA plasmid with a miniprep kit. | Additional, this team transformed plasmids into e. coli in order to amplify plasmids for use by the other teams. This procedure consisted of transforming the plasmid into the bacterial genome, culturing the transformed bacteria, and isolating the DNA plasmid with a miniprep kit. | ||
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Revision as of 03:42, 28 September 2011
Transformation Group
The goal of the transformation team was to successful integrate the four synthesized genes into the yeast genome.
Before the genes were ready, we practiced by transformation by inserting extra DNA into the genome.
When the genes are ligated with the selection markers, we will use the added homology to integrate the linear piece of DNA into the yeast genome. After inserting one gene per yeast cell, we will mate the yeast twice and sporulate in order to isolate the yeast cells that have all four genes present.
Additional, this team transformed plasmids into e. coli in order to amplify plasmids for use by the other teams. This procedure consisted of transforming the plasmid into the bacterial genome, culturing the transformed bacteria, and isolating the DNA plasmid with a miniprep kit.
