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Team:OUC-China/Achievement
From 2013.igem.org
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| - | <div class="col-md-9"><p style="font-weight:normal;"><font size="2px"><a href="https://2013.igem.org/Team:OUC-China/Part description">1.We construct a series of new standard Biobrick part and device and submit it to MIT.</a><br /><br /><a href="https://2013.igem.org/Team:OUC-China/Instruction">2.We design a “RNA guardian” device and prove it matches our goals and submit it to MIT.</a><br /><br />3.We find that Biobrick BBa_K590015 do not work because of the wrong sequence, so we correct it and registry the <i>mam</i>J gene(BBa_K1059014).<br /><br />4.We utilize the microfluidic chip to build the mathematical model reflecting the relationship between the bacterial number and magnetic field intensity.<br /><br />5.We preserved <i>Magnetospirillum Magneticum</i> AMB-1 <i>mam</i>AB genes in <i>E.coli</i>, prevented the genes lose when AMB-1 strain was cultured in high oxygen partial pressure environment.<br /><br /> | + | <div class="col-md-9"><p style="font-weight:normal;"><font size="2px"><a href="https://2013.igem.org/Team:OUC-China/Part description">1.We construct a series of new standard Biobrick part and device and submit it to MIT.</a><br /><br /><a href="https://2013.igem.org/Team:OUC-China/Instruction">2.We design a “RNA guardian” device and prove it matches our goals and submit it to MIT.</a><br /><br />3.We find that Biobrick BBa_K590015 do not work because of the wrong sequence, so we correct it and registry the <i>mam</i>J gene(BBa_K1059014).<br /><br />4.We utilize the microfluidic chip to build the mathematical model reflecting the relationship between the bacterial number and magnetic field intensity.<br /><br />5.We built a model to simulate the route of E.coli in the Microfluidic Chip and quantitatively analyze the magnetic detection ability of the sample bacteria, introducing a magnetism detection coefficient to quantify this ability.<br /><br />6.We preserved <i>Magnetospirillum Magneticum</i> AMB-1 <i>mam</i>AB genes in <i>E.coli</i>, prevented the genes lose when AMB-1 strain was cultured in high oxygen partial pressure environment.<br /><br />7.We help Tsinghua University by constructing a device and sharing drugs.<br /><br />We run lots of human practice activities (see https://2013.igem.org/Team:OUC-China/Human_Practice) to share knowledge and thinking of synthetic biology, discussing and practicing in the usage of biotechnology.<br /><b>We deserve a Gold medal!</b><br /></font></p> |
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Revision as of 02:01, 28 September 2013
Achievement & judge criteria
1.We construct a series of new standard Biobrick part and device and submit it to MIT.
2.We design a “RNA guardian” device and prove it matches our goals and submit it to MIT.
3.We find that Biobrick BBa_K590015 do not work because of the wrong sequence, so we correct it and registry the mamJ gene(BBa_K1059014).
4.We utilize the microfluidic chip to build the mathematical model reflecting the relationship between the bacterial number and magnetic field intensity.
5.We built a model to simulate the route of E.coli in the Microfluidic Chip and quantitatively analyze the magnetic detection ability of the sample bacteria, introducing a magnetism detection coefficient to quantify this ability.
6.We preserved Magnetospirillum Magneticum AMB-1 mamAB genes in E.coli, prevented the genes lose when AMB-1 strain was cultured in high oxygen partial pressure environment.
7.We help Tsinghua University by constructing a device and sharing drugs.
We run lots of human practice activities (see https://2013.igem.org/Team:OUC-China/Human_Practice) to share knowledge and thinking of synthetic biology, discussing and practicing in the usage of biotechnology.
We deserve a Gold medal!
