Team:Cooper Union/Parts

From 2014.igem.org

(Difference between revisions)
Line 59: Line 59:
<h2>Planned Parts</h2>
<h2>Planned Parts</h2>
-
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>
+
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).
-
<!-- De Novo Synthesis - TdT paper with truncated parts improved efficiency
+
<br><br>For De Novo Project, primers for 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>The Programmable Lifespan Timer had a collection of genes knocked out, including EST2, MAK31 and RAD52<br><br>
-
    Programmable Lifespan Timer - Knock out cassettes for EST2, MAK31 and RAD52; Galactosidase inducable CRE Recombinase
+
This summer, four more inputs and outputs were built by The Cooper Union Summer STEM iGEM high school students. The promoters they used were induced by the presence of arsenic, arabinose, lactone and glucose, and the outputs were RFP, YFP, blue chromoprotein, and turquoise chromoprotein. (Over the summer, they worked on dual plasmid systems with real world applications as well. This system could be designed to detect poisons or help control diabetes by measuring glucose levels.)
-
    Biohacker Kit - Assembly of multiple inputs and outputs, as well as different promoters consideration -->
+
<br><br>
 +
 

Revision as of 00:59, 18 October 2014

Cooper Union 2014 iGEM





Tested, Submitted BioBrick Parts


Loading.....


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, primers for 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.

The Programmable Lifespan Timer had a collection of genes knocked out, including EST2, MAK31 and RAD52

This summer, four more inputs and outputs were built by The Cooper Union Summer STEM iGEM high school students. The promoters they used were induced by the presence of arsenic, arabinose, lactone and glucose, and the outputs were RFP, YFP, blue chromoprotein, and turquoise chromoprotein. (Over the summer, they worked on dual plasmid systems with real world applications as well. This system could be designed to detect poisons or help control diabetes by measuring glucose levels.)



Projects Social Notebook Team

Retrieved from "http://2014.igem.org/Team:Cooper_Union/Parts"