Team:Calgary/Project/Acomplishments
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- | The University of Calgary iGEM Team has had many accomplishments this Summer<br><br> | + | <b>The University of Calgary iGEM Team has had many accomplishments this Summer<b><br><br> |
- | In our promoter project | + | <b>In our promoter project...<b><br> |
+ | We designed a novel protocol to identify small hydrophobic molecule interacters. We were able to successfully biotinylate a naphthenic acid, suggesting that we may be able to biotinylate other small hydrophobic molecuels to screen for interactors in the search for sensory elements. <br> | ||
Identified a gene that is upregulated in the presence of NA's, suggesting a possible promoter regions.<br><br> | Identified a gene that is upregulated in the presence of NA's, suggesting a possible promoter regions.<br><br> | ||
In our Reporter Project, we characterized a novel reporter function for the lacZ gene using an electrochemical output.<br><br> | In our Reporter Project, we characterized a novel reporter function for the lacZ gene using an electrochemical output.<br><br> | ||
- | In our Chassis project | + | <b>In our Chassis project...<b><br> |
+ | We characterized a Pseudomonas-E. coli conjugation construct<br> | ||
Submitted parts and protocols for future work in microalgae and Pseudomonas | Submitted parts and protocols for future work in microalgae and Pseudomonas | ||
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Revision as of 10:31, 28 September 2011
Accomplishments
The University of Calgary iGEM Team has had many accomplishments this Summer
In our promoter project...
We designed a novel protocol to identify small hydrophobic molecule interacters. We were able to successfully biotinylate a naphthenic acid, suggesting that we may be able to biotinylate other small hydrophobic molecuels to screen for interactors in the search for sensory elements.
Identified a gene that is upregulated in the presence of NA's, suggesting a possible promoter regions.
In our Reporter Project, we characterized a novel reporter function for the lacZ gene using an electrochemical output.
In our Chassis project...
We characterized a Pseudomonas-E. coli conjugation construct
Submitted parts and protocols for future work in microalgae and Pseudomonas
In our promoter project...
We designed a novel protocol to identify small hydrophobic molecule interacters. We were able to successfully biotinylate a naphthenic acid, suggesting that we may be able to biotinylate other small hydrophobic molecuels to screen for interactors in the search for sensory elements.
Identified a gene that is upregulated in the presence of NA's, suggesting a possible promoter regions.
In our Reporter Project, we characterized a novel reporter function for the lacZ gene using an electrochemical output.
In our Chassis project...
We characterized a Pseudomonas-E. coli conjugation construct
Submitted parts and protocols for future work in microalgae and Pseudomonas