Team:NYMU-Taipei/Our institute

From 2011.igem.org

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*'''<font size=3>Achievements</font>'''
*'''<font size=3>Achievements</font>'''
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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.
*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 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 removed a PstI site of the part BBa_K299806, which express MinC protein. Improve the compacity of this part.
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*We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM.
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*We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM.</font>
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*'''<font size=3>Our institute</font>'''
*'''<font size=3>Our institute</font>'''
*<font size=2>The official web pages of our school - National Yang Ming University (NYMU):
*<font size=2>The official web pages of our school - National Yang Ming University (NYMU):

Revision as of 23:50, 5 October 2011

  • Our design

To achieve this goal, we use a species of magnetic bacteria, Magnetospirillum magneticum AMB-1. We have chosen mms13, a transmembrane protein as our target for protein design in this bacterium, as it serves as a linker between reception of wireless magnetic field and optogenetic neuro-stimulation output. Regarding the neuroimmune response, we choose three genes to achieve symbiosis within glial cell: MinC, a division inhibitor, INV, a gene for invasion and LLO, a gene for facilitated escape from phagosomes.


  • Our design is made up of the following two devices:

  • Achievements

  • 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.
  • Our institute
  • The official web pages of our school - National Yang Ming University (NYMU):
  • Follow the two links below to see The Beauty of NYMU