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| − | <h5>What should this page contain?</h5>
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| − | <li> Clearly and objectively describe the results of your work.</li>
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| − | <li> Future plans for the project. </li>
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| − | <h5>You should also describe what your results mean: </h5>
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| − | <li> Interpretation of the results obtained during your project. Don't just show a plot/figure/graph/other, tell us what you think the data means. This is an important part of your project that the judges will look for. </li>
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| − | <li> Show data, but remember all measurement and characterization data must be on part pages in the Registry. </li>
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| − | <li> Consider including an analysis summary section to discuss what your results mean. Judges like to read what you think your data means, beyond all the data you have acquired during your project. </li>
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| − | <h5> Project Achievements </h5>
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| − | <li>A list of linked bullet points of the successful results during your project</li>
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| − | <li>A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.</li>
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| − | <h5>Inspiration</h5>
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| − | <li><a href="https://2014.igem.org/Team:TU_Darmstadt/Results/Pathway">2014 TU Darmstadt </a></li>
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| − | <li><a href="https://2014.igem.org/Team:Imperial/Results">2014 Imperial </a></li>
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| − | <li><a href="https://2014.igem.org/Team:Paris_Bettencourt/Results">2014 Paris Bettencourt </a></li>
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Revision as of 08:53, 28 October 2017
NTHU_Taiwan
PART I Degradation
1. Cloning of Horseradish Peroxidase
To make sure the plasmid is cloned into E.coli BL-21 strain, we extracted the plasmid from transformed E.coli.(figure 1) We validated the gene by PCR with specific primers and then we examined the result with Agarose gel electrophoresis. A successful cloning was verified from the results of a PCR performed with designed specific primers according to the theoretically expected length of horseradish peroxidase(927bp).
