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Team:Calgary/Notebook/Parts
From 2013.igem.org
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<h2>Parts</h2> | <h2>Parts</h2> | ||
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<p> Here is a summary of all the parts we submitted this year. Details of each part and characterization data can be found on the respective parts.</p></html> | <p> Here is a summary of all the parts we submitted this year. Details of each part and characterization data can be found on the respective parts.</p></html> | ||
| - | <ul><li>We improved two TALE proteins from Slovenia 2012 iGEM team and submitted them in an inducible system. We also designed two TALEs to bind to pathogenic <i>E. coli </i> genomic sequences. </li> | + | <ul><li>We improved two TALE proteins from Slovenia 2012 iGEM team and submitted them in an inducible system (LacI) and with a his-6 tag such that they can be easily expressed and purified. </li> |
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| + | <li>We also designed two TALEs to bind to pathogenic <i>E. coli </i> genomic sequences. </li> | ||
| - | <li>We submitted the E and K coils which can be used as connector for scaffolding proteins that cannot be fused together</li> | + | <li>We submitted the E and K coils which can be used as connector for scaffolding proteins that cannot be fused together. We submitted these coils in the Friedburg assembly backbone such that other teams can easily create fusion proteins with them.</li> |
| - | <li> We submitted two new reporters: Beta-Lactamase and Ferritin to the registry. We also submitted these with his tag and in an inducible system (LacI). </li> | + | <li> We submitted two new reporters: Beta-Lactamase and Ferritin to the registry. We also submitted these with his-6 tag and in an inducible system (LacI) such that they are easy to express and isolate. </li></ul> |
<groupparts>iGEM013 Calgary</groupparts> | <groupparts>iGEM013 Calgary</groupparts> | ||
Revision as of 00:38, 28 September 2013
Parts
Parts
Here is a summary of all the parts we submitted this year. Details of each part and characterization data can be found on the respective parts.
- We improved two TALE proteins from Slovenia 2012 iGEM team and submitted them in an inducible system (LacI) and with a his-6 tag such that they can be easily expressed and purified.
- We also designed two TALEs to bind to pathogenic E. coli genomic sequences.
- We submitted the E and K coils which can be used as connector for scaffolding proteins that cannot be fused together. We submitted these coils in the Friedburg assembly backbone such that other teams can easily create fusion proteins with them.
- We submitted two new reporters: Beta-Lactamase and Ferritin to the registry. We also submitted these with his-6 tag and in an inducible system (LacI) such that they are easy to express and isolate.
<groupparts>iGEM013 Calgary</groupparts>
