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Team:NYMU-Taipei/Our institute
From 2011.igem.org
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*'''<font size=3>Achievements</font>''' | *'''<font size=3>Achievements</font>''' | ||
<font size=2> | <font size=2> | ||
| - | *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. | + | *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. | + | *2.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. | + | *3.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. | + | *4.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.</font> | + | *5.We designed a free online software, which provides an automated ONE-STEP primer design service of BioBricks for iGEM.</font> |
*'''<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 23:58, 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:
- Optomagnetic Design
- Bridge magnetics and optogenetics
- Immunological Solution
- Make magnetic bacteria symbiosis with glia cell
- Achievements
- 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.
- 2.We submitted over 60 parts to the resgristry, which can be used for application magnetic enlightment, cloning AMB-1, Symbiosis with Human cell.
- 3.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.
- 4.We removed a PstI site of the part BBa_K299806, which express MinC protein. Improve the compacity of this part.
- 5.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):
- [http://web.ym.edu.tw/front/bin/home.phtml in Chinese]
- [http://nymu-e.web.ym.edu.tw/front/bin/home.phtml in English]
- Follow the two links below to see The Beauty of NYMU
- [http://issue.ym.edu.tw/cia/new/ Take a panoramic scenery view of our university]
- [http://issue.ym.edu.tw/cia/new/tw/ym720.html Take a tour of our university]
