Team:HKUST/Result3
From 2009.igem.org
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- | <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 Production</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/ToxinProduction">Toxin Production</a></li> | ||
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<p>Constructs </p> | <p>Constructs </p> | ||
- | We have successfully cloned the FUS1t gene into the multiple cloning site of the | + | 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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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.