Team:OUC-China

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Latest revision as of 03:59, 18 October 2014

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-<img class="logo" src="https://static.igem.org/mediawiki/2014/c/c6/OUC-China_Content_IGEM.png" style="left:10px" />
+<a href="https://igem.org/Main_Page"><img class="logo" src="https://static.igem.org/mediawiki/2014/c/c6/OUC-China_Content_IGEM.png" style="left:10px" /></a>
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          <ul style="margin-top:-100px">
              <li><a href="https://2014.igem.org/Team:OUC-China/Safety">Biosafety</a></li>
-             <li><a href="https://2014.igem.org/Team:OUC-China/Safety_Lab_Safety">Labsafety</a></li>
+             <li><a href="https://2014.igem.org/Team:OUC-China/Safety_Lab_safety">Labsafety</a></li>
              <li style="border-bottom-left-radius:5px;border-bottom-right-radius:5px"><a style="font-size:22px">SAFETY</a></li>
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+            </li>
+            <li>
+<img src="https://static.igem.org/mediawiki/2014/5/58/OUC-China_Index_Slide4.png" style="width:80%;margin:80px auto;display:block;position:inherit" />
+            </li>
+            <li>
+<img src="https://static.igem.org/mediawiki/2014/2/2f/OUC-China_Index_Slide5.png" style="width:80%;margin:80px auto;display:block;position:inherit" />
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-<h2 class="text-primary" style="width:1210px;margin:0 auto;padding-top:10px;">Introduction</h2>
+<h2 class="text-primary" style="width: 960px;margin:0 auto;padding-top:10px;">Introduction</h2>
-<p style="width:1210px;margin:0 auto;font-size:16px;padding-top:12px;">Generally, researchers transfer plasmids from prokaryote to eukaryote by non-autonomous methods, while we manage to make plasmid transfer by autonomous and convenient methods. This year, OUC-China iGEM devotes to design a novel model of plasmid transfer. Because the plasmid can't transfer into natural bacteria easily in vivo, we transport the plasmid into the organism with a double plasmid system, and then the constructed plasmid that has lysis device can transfer to the dominant colony in organism by conjugation. Afterwards, the dominant colony with constructed plasmid can lysis and release the constructed plasmid and a fusion protein composed of cationic TAT peptide and histone H4 that we designed. The protein complex will carry the constructed plasmid into eukaryote to operate. The aim of the project is to construct a novel model method of eukaryotic transfection for molecular biology research at individual level, such as DNA vaccine and molecular marker.</p>
+<p style="width: 960px;margin:0 auto;font-size: 19px;padding-top:12px;">Current researches usually transfer exogenous DNA into prokaryotic cells and eukaryotic cells, while OUC-China iGEM team has designed an innovative method to carry exogenous DNA from prokaryote to eukaryota more efficiently. Eventually we have applied the method to studies of the model organism, zebrafish. <br />
-<a href="https://2014.igem.org/Team:OUC-China/Project" class="btn btn-primary" style="display:block;margin:40px auto;width:200px;position:relative;">Learn More</a>
+We have constructed the fusion protein that can bind and protect plasmids, with the ability of helping plasmids transfect into eukaryotic cells in high efficiency.</p>
+<a href="https://2014.igem.org/Team:OUC-China/Project" class="btn btn-primary btn-lg" style="display:block;margin:40px auto;width:200px;position:relative;color: #ffffff;">Learn More</a>
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-         <p style="top: 231px; left: 69px;"><a href="https://2014.igem.org/Team:OUC-China/Safety_Policy_Practise">Policy&Practise </a></p>
+         <p style="top: 231px; left: 69px;"><a href="https://2014.igem.org/Team:OUC-China/Project_Policy_Practise">Policy&Practise </a></p>
        </li>
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+    .footer > p { text-align: center; color: #ffffff }
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+    <img src="https://static.igem.org/mediawiki/2014/a/ad/OUC-China_Index_OrgLogo.png" />
+    <img src="https://static.igem.org/mediawiki/2014/e/ec/OUC-China_Index_OrgTitle.jpg" />
+    <img src="https://static.igem.org/mediawiki/2014/9/96/OUC-China_Foot_ouclogo.png" />
+    <div style="clear:both"></div>
+  </div>
+  <p>contact us: <a href="mailto:oucigem@163.com">oucigem@163.com</a></p>
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