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Team:NYMU-Taipei/results/achievements
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| + | ==Achievements== | ||
| + | *We designed a new cloning vector for AMB-1 which is compatible with common BioBricks, making it easier for iGEMers to clone into the magnetic bacteria AMB-1. | ||
| + | *We submitted over 60 parts to the registry, which can be used for applications of magnetic enlightment, cloning AMB-1, and Symbiosis with Human cells. | ||
| + | *We designed helical anti-membrane protein CHAMP for mms13, separating the two helices of the magnetite binding protein mms13 and making it a flexible part for the use of magnetic field in iGEM. | ||
| + | *We removed a PstI site from the part BBa_K299806, a part which expresses the MinC protein. We improved the compacity of this part. | ||
| + | *We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM. | ||
| + | </font> | ||
Latest revision as of 01:20, 6 October 2011
Achievements
- We designed a new cloning vector for AMB-1 which is compatible with common BioBricks, making it easier for iGEMers to clone into the magnetic bacteria AMB-1.
- We submitted over 60 parts to the registry, which can be used for applications of magnetic enlightment, cloning AMB-1, and Symbiosis with Human cells.
- We designed helical anti-membrane protein CHAMP for mms13, separating the two helices of the magnetite binding protein mms13 and making it a flexible part for the use of magnetic field in iGEM.
- We removed a PstI site from the part BBa_K299806, a part which expresses the MinC protein. We improved the compacity of this part.
- We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM.
