"
Team:Berkeley/Attributions
From 2012.igem.org
| Line 43: | Line 43: | ||
<br> | <br> | ||
<p> | <p> | ||
| - | Many of our basic parts (promoters, terminators, RBSs, and fluorescent proteins) are courtesy of the Dueber lab. | + | <b>Wetlab</b> |
| - | + | <p> | |
| + | Many of our basic parts (promoters, terminators, RBSs, and fluorescent proteins) are courtesy of the <a href="http://dueberlab.berkeley.edu/">Dueber Lab</a>, our host lab. | ||
| + | |||
<p> | <p> | ||
The iGEM team chose the targeting proteins/sequences from the literature and either PCRed them from genomic DNA or synthesized them, built all of the composite parts, and assayed them. | The iGEM team chose the targeting proteins/sequences from the literature and either PCRed them from genomic DNA or synthesized them, built all of the composite parts, and assayed them. | ||
| - | + | ||
<p> | <p> | ||
| - | The leucine zipper sequences were courtesy of | + | The leucine zipper sequences were courtesy of the <a href="http://web.mit.edu/biology/keating/KeatingLab/Home.html"> |
| - | + | Keating Lab</a> at MIT, in a collaborative effort to identify an orthogonal interaction set. The iGEM team constructed the MiCoded leucine zippers and assayed them. | |
| + | |||
<p> | <p> | ||
The Golden Gate assembly of our multigene and MiCode cassettes was designed and performed by the iGEM team. | The Golden Gate assembly of our multigene and MiCode cassettes was designed and performed by the iGEM team. | ||
| - | < | + | |
| + | <b>Computational</b> | ||
<p> | <p> | ||
On the software side, the iGEM team wrote the MATLAB code, constructed the Cell Profiler pipeline for automated image analysis, and tested it using images generated by the iGEM team. | On the software side, the iGEM team wrote the MATLAB code, constructed the Cell Profiler pipeline for automated image analysis, and tested it using images generated by the iGEM team. | ||
| + | <p> | ||
| + | |||
| + | <b>Website</b> | ||
| + | <p> | ||
| + | With their permission, we began with the template of <a href="https://2011.igem.org/Team:Berkeley">Berkeley iGEM 2011</a>, and tweaked it to our needs this year. | ||
</p> | </p> | ||
</html> | </html> | ||
Revision as of 07:13, 29 September 2012
Wetlab
Many of our basic parts (promoters, terminators, RBSs, and fluorescent proteins) are courtesy of the Dueber Lab, our host lab.
The iGEM team chose the targeting proteins/sequences from the literature and either PCRed them from genomic DNA or synthesized them, built all of the composite parts, and assayed them.
The leucine zipper sequences were courtesy of the Keating Lab at MIT, in a collaborative effort to identify an orthogonal interaction set. The iGEM team constructed the MiCoded leucine zippers and assayed them.
The Golden Gate assembly of our multigene and MiCode cassettes was designed and performed by the iGEM team. Computational
On the software side, the iGEM team wrote the MATLAB code, constructed the Cell Profiler pipeline for automated image analysis, and tested it using images generated by the iGEM team.
Website
With their permission, we began with the template of Berkeley iGEM 2011, and tweaked it to our needs this year.
