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Team:HKUST/Result3
From 2009.igem.org
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<li><a href="https://2009.igem.org/Team:HKUST">Home</a></li> | <li><a href="https://2009.igem.org/Team:HKUST">Home</a></li> | ||
<li><a href="https://2009.igem.org/Team:HKUST/Team">Our Team</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/Team">Our Team</a></li> | ||
| - | <li><a href="https://2009.igem.org/Team:HKUST/Project">Project | + | <li><a href="https://2009.igem.org/Team:HKUST/Project">Project Description</a></li> |
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</span> | </span> | ||
</b> | </b> | ||
| - | <li><a href="https://2009.igem.org/Team:HKUST/ | + | <li><a href="https://2009.igem.org/Team:HKUST/OdorantSensing">Odorant Sensing</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/ | + | <li><a href="https://2009.igem.org/Team:HKUST/AttractantProduction">Attractant Production</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin | + | <li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin Production</a></li> |
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<li><a href="https://2009.igem.org/Team:HKUST/Lab Notebook">Lab Notebook</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/Lab Notebook">Lab Notebook</a></li> | ||
<li><a href="https://2009.igem.org/Team:HKUST/Parts">Parts Submitted </a></li> | <li><a href="https://2009.igem.org/Team:HKUST/Parts">Parts Submitted </a></li> | ||
| - | <li><a href="https://2009.igem.org/Team:HKUST/Protocols">Protocol | + | <li><a href="https://2009.igem.org/Team:HKUST/Protocols">Protocol List</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/Resourses">Other | + | <li><a href="https://2009.igem.org/Team:HKUST/Resourses">Other Resources</a></li> |
</ul> | </ul> | ||
</div> | </div> | ||
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<ul> | <ul> | ||
<li><a href="https://2009.igem.org/Team:Gallery">Gallery</a></li> | <li><a href="https://2009.igem.org/Team:Gallery">Gallery</a></li> | ||
| - | <li><a href="https://2009.igem.org/Team: | + | <li><a href="https://2009.igem.org/Team:Biosafety">Biosafety</a></li> |
<li><a href="https://2009.igem.org/Team:Acknowledgement">Acknowledgement</a></li> | <li><a href="https://2009.igem.org/Team:Acknowledgement">Acknowledgement</a></li> | ||
</ul> | </ul> | ||
</div> | </div> | ||
</div> | </div> | ||
| - | <div id="rightxx"> | + | <div id="rightxx"> |
| + | <div class="contentatt_re"> <h3>a</h3> | ||
| + | </div> | ||
<div class="contentxx"> | <div class="contentxx"> | ||
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| + | <p>Constructs </p> | ||
| + | We have successfully cloned the FUS1t gene into the multiple cloning site of the vector pRS426. Agarose gel electrophoresis shows correct sizes after enzyme digestion of pRS426-tFUS1. The other parts, the FUS1 promoter and the EGFP gene are still under construction. Also, the ARO9 gene has been amplified from the yeast genome.</p> | ||
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<br> | <br> | ||
<br> | <br> | ||
<li><a href="https://2009.igem.org/Team:HKUST/Back3">Background</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/Back3">Background</a></li> | ||
| - | <li><a href="https://2009.igem.org/Team:HKUST/Group3">Experimental | + | <li><a href="https://2009.igem.org/Team:HKUST/Group3">Experimental Design</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/Part3">Parts | + | <li><a href="https://2009.igem.org/Team:HKUST/Part3">Parts Design</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/Result3">Experimental | + | <li><a href="https://2009.igem.org/Team:HKUST/Result3">Experimental Results</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/Future3">Future | + | <li><a href="https://2009.igem.org/Team:HKUST/Future3">Future Work</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/Ref3"> | + | <li><a href="https://2009.igem.org/Team:HKUST/Ref3">References</a></li> |
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<span> iGEM 2009 <br /> </span> | <span> iGEM 2009 <br /> </span> | ||
</div> | </div> | ||
| - | <div id="payment"><img src="http://igem2009hkust.fileave.com/wiki/template/12092009/images/HKUSTLogo.jpg" alt=" | + | <div id="payment"><img src="http://igem2009hkust.fileave.com/wiki/template/12092009/images/HKUSTLogo.jpg" alt="HKUST" /></div> |
</div> | </div> | ||
<div id="footerend"></div> | <div id="footerend"></div> | ||
Latest revision as of 19:06, 21 October 2009
a
Constructs
We have successfully cloned the FUS1t gene into the multiple cloning site of the vector pRS426. Agarose gel electrophoresis shows correct sizes after enzyme digestion of pRS426-tFUS1. The other parts, the FUS1 promoter and the EGFP gene are still under construction. Also, the ARO9 gene has been amplified from the yeast genome.
iGEM 2009
