Difference between revisions of "Team:SDU CHINA"

 
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{{SDU_CHINA}}
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    <div class="image" ><img src="bottom.jpg" width=100%/></div>
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    <div class="bar"><p style="text-align:center;font-size:34px">NAVIGATION</p></div>
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    <div class="title"><b>SDU_CHINA</b></div>
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<img src="https://static.igem.org/mediawiki/2017/4/4c/Bg.jpeg" style="width:100%;height:auto" style="width:100%;height:auto">
 
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<div class="c"><img src="https://static.igem.org/mediawiki/2017/9/92/Abstract.jpeg" style="width:100%;height:auto"></div>
  
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    <div class="title"><h4>Abstract</h4></div>
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    <div class="content"><p>The incidence of cancer is increasing in modern
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<div class="video" style="background:url('https://static.igem.org/mediawiki/2017/5/55/Bggg.jpeg');background-size:100%;padding-top:12em;height:480px;background-repeat:none">
    society. In all cancer patients, P53 mutations account for nearly 50%.  
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<video src="https://static.igem.org/mediawiki/2017/1/10/Video.mp4" width="48%" controls="controls">
    If the mutant P53 can be replaced with wild P53 using gene therapy method,
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      it will be the best theropy for those patients. In our project, we are
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      using CRISPR technique to cut the mutant p53 in tumor cells. In the pro
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      cess of genome repair, wild p53 will be integrated into genome via the
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      principle of homologous recombination, restructuring the genome of cancer
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      cells so as to realize the replacement of mutant p53. The
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      characteristics of our project is that after the mutant p53 is replaced,
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        the transfected plasmids will commit suicide. Even if the plasmids are
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        transfected into the nontumorous cells, plasmids will also cut and
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        degrade themselves. So it will not pose a threat to normal cells,
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        achieving the safety of gene therapy.</p></div>
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    <div class="icon" > <img src="archive_128px_1207992_easyicon.net.png"> </div>
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Latest revision as of 05:07, 31 October 2017

SDU_CHINA