Team:Cooper Union/Parts

From 2014.igem.org

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<h2>Planned Parts</h2>
<h2>Planned Parts</h2>
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The scope of our project may be vast, but we only submitted parts we were able to successfully characterize. A lot of other components were considered from each sub-project that did not make it due to time constraints (and a bit of Murphy's Law).<br><br>
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The scope of our project may be vast, but we only submitted parts we were able to successfully characterize. A lot of other components were considered from each sub-project that did not make it due to time constraints (and a bit of Murphy's Law). For De novo Project, truncated TdT enzymes with the Biobrick prefixes were synthesized and used. Referring to the literature, first 81bp, 429bp, and 450bp of TdT were deleted to see the change in efficiency of the TdT's enzymatic function. <br><br>
<!-- De Novo Synthesis - TdT paper with truncated parts improved efficiency  
<!-- De Novo Synthesis - TdT paper with truncated parts improved efficiency  
     Programmable Lifespan Timer - Knock out cassettes for EST2, MAK31 and RAD52; Galactosidase inducable CRE Recombinase
     Programmable Lifespan Timer - Knock out cassettes for EST2, MAK31 and RAD52; Galactosidase inducable CRE Recombinase

Revision as of 00:26, 18 October 2014

Cooper Union 2014 iGEM






Tested, Submitted BioBrick Parts


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Planned Parts

The scope of our project may be vast, but we only submitted parts we were able to successfully characterize. A lot of other components were considered from each sub-project that did not make it due to time constraints (and a bit of Murphy's Law). For De novo Project, truncated TdT enzymes with the Biobrick prefixes were synthesized and used. Referring to the literature, first 81bp, 429bp, and 450bp of TdT were deleted to see the change in efficiency of the TdT's enzymatic function.