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<h3>Safety of Our Project</h3> | <h3>Safety of Our Project</h3> | ||
− | <p>Before releasing works, we had made sure our operations met all the safety requirements and granted by the University. The University of Edinburgh Biological Safety Committee had created a safe system that would allow us to achieve our goals. For each of us, basic steps of individual project started with gene amplification, and went for cutting-and-ligating, then went for transforming into E. coli and went for bacterial culturing. </p> | + | <p>Before releasing works, we had made sure our operations met all the safety requirements and granted by the University. The University of Edinburgh Biological Safety Committee had created a safe system that would allow us to achieve our goals. For each of us, basic steps of individual project started with gene amplification, and went for cutting-and-ligating, then went for transforming into <em>E. coli</em> and went for bacterial culturing. </p> |
<p>Compositions for plasmids constructing and parts building were partly from iGEM 2018 distribution kits with valid registry numbers, for example, we used the plasmid backbone pSB3T5 and pSB1C3, the previous parts BBa_K1149051, the rest gene fragments came from PCR or Gibson assemblies, which are native in <em>E. coli</em> DH5a and were transformed into <em>E. coli</em> BL21DE3.</p> | <p>Compositions for plasmids constructing and parts building were partly from iGEM 2018 distribution kits with valid registry numbers, for example, we used the plasmid backbone pSB3T5 and pSB1C3, the previous parts BBa_K1149051, the rest gene fragments came from PCR or Gibson assemblies, which are native in <em>E. coli</em> DH5a and were transformed into <em>E. coli</em> BL21DE3.</p> |
Revision as of 13:12, 17 October 2018