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Team:HKUST-Hong Kong/Parts and Device
From 2012.igem.org
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<h1>Overview</h1> | <h1>Overview</h1> | ||
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| - | <p>The | + | <p>The HKUST iGEM 2012 team has submitted 18 BioBricks in total. <a href="https://static.igem.org/mediawiki/2012/7/73/Parts_and_Device.pdf" target="_blank">A full list of BioBricks</a> has been attached with this page.<br /> |
| - | For the | + | For the Target Binding module, two BioBricks were built to display the colon tumor recognition peptide, RPMrel, on the cell wall of <i>B. subtilis</i>. In the Anti-tumor molecule synthesis module, two BioBricks are built for BMP2 synthesis and secretion whiel the other five were built to facilitate the accomplishment of BMP2 synthesis. 11 Biobricks are built for cell growth inhibitory module. They are mainly used to driven the toxin-antitoxin system and control the expression of BMP2.<a href="https://static.igem.org/mediawiki/2012/e/ee/Sorted_by_Module.pdf" target="_blank"> They are sorted by module as shown in this page.</a><br /> |
Among all 18 parts, three of them are well characterized. They are <a href="http://partsregistry.org/Part:BBa_K733009">BBa_K733009</a>, a GFP generator driven by pTms promoter; <a href="http://partsregistry.org/Part:BBa_K733018" target="_blank">BBa_K733018</a>, a GFP generator driven by xylose inducible promoter and <a href="http://partsregistry.org/Part:BBa_K733012" target="_blank">BBa_K733012</a>, the cell growth inhibitory device. For detailed <a href="https://2012.igem.org/Team:HKUST-Hong_Kong/Characterization">characterization</a> data please refer to the information of these three biobricks or our characterization section on wiki.<br /> | Among all 18 parts, three of them are well characterized. They are <a href="http://partsregistry.org/Part:BBa_K733009">BBa_K733009</a>, a GFP generator driven by pTms promoter; <a href="http://partsregistry.org/Part:BBa_K733018" target="_blank">BBa_K733018</a>, a GFP generator driven by xylose inducible promoter and <a href="http://partsregistry.org/Part:BBa_K733012" target="_blank">BBa_K733012</a>, the cell growth inhibitory device. For detailed <a href="https://2012.igem.org/Team:HKUST-Hong_Kong/Characterization">characterization</a> data please refer to the information of these three biobricks or our characterization section on wiki.<br /> | ||
To convenient the future iGEM team in using and searching for biobricks, we also sorted our biobricks based on their type. <a target="_blank" href="https://static.igem.org/mediawiki/2012/d/d0/Sorted_by_Type.pdf">Detailed information please refer to here.</a></p> | To convenient the future iGEM team in using and searching for biobricks, we also sorted our biobricks based on their type. <a target="_blank" href="https://static.igem.org/mediawiki/2012/d/d0/Sorted_by_Type.pdf">Detailed information please refer to here.</a></p> | ||
Revision as of 16:10, 26 September 2012
Parts and Devices
Overview
The HKUST iGEM 2012 team has submitted 18 BioBricks in total. A full list of BioBricks has been attached with this page.
For the Target Binding module, two BioBricks were built to display the colon tumor recognition peptide, RPMrel, on the cell wall of B. subtilis. In the Anti-tumor molecule synthesis module, two BioBricks are built for BMP2 synthesis and secretion whiel the other five were built to facilitate the accomplishment of BMP2 synthesis. 11 Biobricks are built for cell growth inhibitory module. They are mainly used to driven the toxin-antitoxin system and control the expression of BMP2. They are sorted by module as shown in this page.
Among all 18 parts, three of them are well characterized. They are BBa_K733009, a GFP generator driven by pTms promoter; BBa_K733018, a GFP generator driven by xylose inducible promoter and BBa_K733012, the cell growth inhibitory device. For detailed characterization data please refer to the information of these three biobricks or our characterization section on wiki.
To convenient the future iGEM team in using and searching for biobricks, we also sorted our biobricks based on their type. Detailed information please refer to here.
