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<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 | + | <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. The Proof of Concept results can be found on our <a href="https://2017.igem.org/Team:TU-Eindhoven/Demonstrate">“Demonstrate”</a> page.</br></br> |
As iGEM is a broad competition based around synthetic biology, we also did many other things, for example thinking about safety and the future, which are part of <a href="https://2017.igem.org/Team:TU-Eindhoven/Human_Practices">“Human Practices”</a>. </br></br> | As iGEM is a broad competition based around synthetic biology, we also did many other things, for example thinking about safety and the future, which are part of <a href="https://2017.igem.org/Team:TU-Eindhoven/Human_Practices">“Human Practices”</a>. </br></br> |
Revision as of 15:32, 1 November 2017