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Team:NYMU-Taipei/results/achievements
From 2011.igem.org
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*We designed a new cloning vector of AMB-1 which is compatible with common biobricks, make it easier for igemers to clone magnetic bacteria AMB-1. | *We designed a new cloning vector of AMB-1 which is compatible with common biobricks, make it easier for igemers to clone magnetic bacteria AMB-1. | ||
*We submitted over 60 parts to the resgristry, which can be used for application magnetic enlightment, cloning AMB-1, Symbiosis with Human cell. | *We submitted over 60 parts to the resgristry, which can be used for application magnetic enlightment, cloning AMB-1, Symbiosis with Human cell. | ||
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*We removed a PstI site of the part BBa_K299806, which express MinC protein. Improve the compacity of this part. | *We removed a PstI site of the part BBa_K299806, which express MinC protein. Improve 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 23:44, 5 October 2011
- We designed a new cloning vector of AMB-1 which is compatible with common biobricks, make it easier for igemers to clone magnetic bacteria AMB-1.
- We submitted over 60 parts to the resgristry, which can be used for application magnetic enlightment, cloning AMB-1, Symbiosis with Human cell.
- We designed helical anti-membrane protein CHAMP for mms13, seperate two helix of magnetite binding protein mms13. Make it a flexible use of magnetic field in iGEM.
- We removed a PstI site of the part BBa_K299806, which express MinC protein. Improve the compacity of this part.
- We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM.
