"
Team:uOttawa/Results
From 2011.igem.org
(Difference between revisions)
| Line 5: | Line 5: | ||
</html> | </html> | ||
| + | |||
| + | == BioBrick characterization == | ||
| + | |||
| + | '''Characterization of BBa_K642000 and BBa_K642004''' | ||
| + | We quantified the fluorescence of two tagged repressors: BBa_K642000 and BBa_K642004 by cloning them downstream of the yeast Gal10/1 promoter. The construct was then integrated using KanMX6 selection into the Ade2 locus of a BY4742 strain of S.cerevisiae. The resulting strain was innoculated in 3 mL of 1x SM + 2% Galactose + 2% Adenine overnight. The overnight culture was reinoculated into 1 mL of the same media at an OD600 of 0.02. After three hours the strain was analyzed for BFP fluorescence on a Cyan ADP flow cytometer. | ||
| + | |||
| + | [[File:BFP_graph.jpg]] | ||
{{Template:uOttawa_Footer}} | {{Template:uOttawa_Footer}} | ||
Revision as of 02:30, 29 September 2011
Results
BioBrick characterization
Characterization of BBa_K642000 and BBa_K642004 We quantified the fluorescence of two tagged repressors: BBa_K642000 and BBa_K642004 by cloning them downstream of the yeast Gal10/1 promoter. The construct was then integrated using KanMX6 selection into the Ade2 locus of a BY4742 strain of S.cerevisiae. The resulting strain was innoculated in 3 mL of 1x SM + 2% Galactose + 2% Adenine overnight. The overnight culture was reinoculated into 1 mL of the same media at an OD600 of 0.02. After three hours the strain was analyzed for BFP fluorescence on a Cyan ADP flow cytometer.
