Team:NYMU-Taipei/results/achievements

From 2011.igem.org

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(Achievements)
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==Achievements==
==Achievements==
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*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.
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*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 submitted over 60 parts to the registry, which can be used for applications of magnetic enlightment, cloning AMB-1, and Symbiosis with Human cells.
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*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.
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*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.
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*We removed a PstI site from the part BBa_K299806, which express the MinC protein. Improved the compacity of this part.
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*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.
*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 01:20, 6 October 2011

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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.