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Team:NYMU-Taipei/results/achievements
From 2011.igem.org
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==Achievements== | ==Achievements== | ||
| - | *We designed a new cloning vector | + | *We designed a new cloning vector for AMB-1 which is compatible with common biobricks (Assembly Standard 10), making it easier for iGEMers to clone into the magnetic bacteria AMB-1. |
| - | *We submitted over 60 parts to the | + | *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, | + | *We designed helical anti-membrane protein CHAMP for mms13, separating the two helices of magnetite binding protein mms13 and making it a flexible part for use of magnetic field in iGEM. |
| - | *We removed a PstI site | + | *We removed a PstI site from the part BBa_K299806, which express the MinC protein. 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. | *We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM. | ||
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Revision as of 01:09, 6 October 2011
Achievements
- We designed a new cloning vector for AMB-1 which is compatible with common biobricks (Assembly Standard 10), 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 magnetite binding protein mms13 and making it a flexible part for use of magnetic field in iGEM.
- We removed a PstI site from the part BBa_K299806, which express the MinC protein. 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.
