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+ | <h2>The TU Eindhoven team of 2017 has won a golden medal and was nominated for Best New Application!</h2> | ||
<h1>Overview of generated results</h1> | <h1>Overview of generated results</h1> | ||
<h6>During iGEM we generated many different sorts of results. In the beginning of iGEM we mostly worked on getting the right DNA plasmids, by using different methods, like Gibson assembly and Traditional Cloning. In this period, the most important results included agarose gels and sequencing result (they are presented in <a href="https://2017.igem.org/Team:TU-Eindhoven/Results/DNA">"DNA results"</a>). After this period, we had to test the expression of our designed proteins and instead of agarose gels, SDS-PAGE gels became more important. The last period is marked by the "real" experiments, where we could finally test if our designed system indeed worked as planned. To get an overview of all the steps we performed in the lab, go see our <a href="https://2017.igem.org/Team:TU-Eindhoven/Team/Notebook">"Notebook"</a> page. <br/><br/> | <h6>During iGEM we generated many different sorts of results. In the beginning of iGEM we mostly worked on getting the right DNA plasmids, by using different methods, like Gibson assembly and Traditional Cloning. In this period, the most important results included agarose gels and sequencing result (they are presented in <a href="https://2017.igem.org/Team:TU-Eindhoven/Results/DNA">"DNA results"</a>). After this period, we had to test the expression of our designed proteins and instead of agarose gels, SDS-PAGE gels became more important. The last period is marked by the "real" experiments, where we could finally test if our designed system indeed worked as planned. To get an overview of all the steps we performed in the lab, go see our <a href="https://2017.igem.org/Team:TU-Eindhoven/Team/Notebook">"Notebook"</a> page. <br/><br/> |
Latest revision as of 10:18, 15 December 2017