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Team:TU-Eindhoven/LEC/BioBricks
From 2012.igem.org
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<p>The permission we needed to add the GECO’s to registry library was not easy to get. You can read more about this struggle at the Considerations-page.</p> | <p>The permission we needed to add the GECO’s to registry library was not easy to get. You can read more about this struggle at the Considerations-page.</p> | ||
{{:Team:TU-Eindhoven/Templates/footer}} | {{:Team:TU-Eindhoven/Templates/footer}} | ||
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| + | <h3>Characterization</h3> | ||
| + | =Growth Rate and Expression= | ||
| + | [[Image:Growth_rate.JPG|500px|right|link=]] | ||
| + | E. Coli strain BL21 transformed with Part BBa_K881000 and Part BBa_K881001 ligated into vector pET_28a were cultured in LB media containing 100 µg/ml kanamycin for ~4 hours at 37°C. The growth rate was followed by use of OD600 measurements (see figure on the right). Then the culture was induced at an OD600 of 0,82 absorption units with 100 µg/ml IPTG. | ||
Revision as of 19:45, 25 September 2012
BioBricks
The GECO’s, R-GECO (red), G-GECO (green) and B-GECO (blue) are the biobricks we will send to the registry. Those biobricks can be used in yeast and in E.coli cells. The protocol attached with the biobrick-library didn’t work for us. We used our own restriction and ligation protocols to develop the biobrick.
The permission we needed to add the GECO’s to registry library was not easy to get. You can read more about this struggle at the Considerations-page.
Characterization
Growth Rate and Expression
E. Coli strain BL21 transformed with Part BBa_K881000 and Part BBa_K881001 ligated into vector pET_28a were cultured in LB media containing 100 µg/ml kanamycin for ~4 hours at 37°C. The growth rate was followed by use of OD600 measurements (see figure on the right). Then the culture was induced at an OD600 of 0,82 absorption units with 100 µg/ml IPTG.
