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Team:HKUST/Result3
From 2009.igem.org
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<li><a href="https://2009.igem.org/Team:HKUST/Project">Project description</a></li> | <li><a href="https://2009.igem.org/Team:HKUST/Project">Project description</a></li> | ||
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| - | <li> | + | <li>Main Parts</li> |
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| - | <li><a href="https://2009.igem.org/Team:HKUST/ | + | <li><a href="https://2009.igem.org/Team:HKUST/OdorantSensoring">Odorant sensoring</a></li> |
| - | <li><a href="https://2009.igem.org/Team:HKUST/ | + | <li><a href="https://2009.igem.org/Team:HKUST/AttranctantProduction">Attranctant production</a></li> |
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| - | <li> | + | <li>Resources</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> | ||
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<h3>Welcome</h3> | <h3>Welcome</h3> | ||
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<p>Constructs </p> | <p>Constructs </p> | ||
We have successfully cloned the FUS1t gene into the multiple cloning site of the plasmid pRS426. The agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1 is shown in Figure 6. The other parts, the FUS1 promoter and the EGFP gene are still under construction. Also, the ARO9 gene has been amplified from yeast genome.</p> | We have successfully cloned the FUS1t gene into the multiple cloning site of the plasmid pRS426. The agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1 is shown in Figure 6. The other parts, the FUS1 promoter and the EGFP gene are still under construction. Also, the ARO9 gene has been amplified from yeast genome.</p> | ||
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Figure 6 agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1 | Figure 6 agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1 | ||
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| + | <li><a href="https://2009.igem.org/Team:HKUST/Back3">Background</a></li> | ||
| + | <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 design</a></li> | ||
| + | <li><a href="https://2009.igem.org/Team:HKUST/Result3">Experimental result</a></li> | ||
| + | <li><a href="https://2009.igem.org/Team:HKUST/Future3">Future work</a></li> | ||
| + | <li><a href="https://2009.igem.org/Team:HKUST/Ref3">Reference</a></li> | ||
Revision as of 11:20, 17 October 2009
Welcome
Constructs
We have successfully cloned the FUS1t gene into the multiple cloning site of the plasmid pRS426. The agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1 is shown in Figure 6. The other parts, the FUS1 promoter and the EGFP gene are still under construction. Also, the ARO9 gene has been amplified from yeast genome. Figure 6 agarose gel electrophoresis pictures showing the correct sizes after enzyme digestion of pRS426-tFUS1
iGEM 2009
