Team:Freiburg/Content/Team/Members

From 2014.igem.org

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<p>We succeed to stably integrate our gene of interest into the genome of target cells by using a viral vector derived from the murine leukemia virus. The advantages of this vector are: its specificity for murine cells, making the viral work safe and easy; a very high efficiency for infection; and the ability of stable gene transfer into the genomes of target cells. Here we present results on these three qualities of our viral vector and how we optimized virus production and cell infection.</p>
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<p>This is one of our members and here you can read something about him in the future</p>
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<p>This is also one of our members and soon you will get some more information about her</p>
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<h1>Team</h1>
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<li><a href="/Team:Freiburg/Team/Members">Members</a></li><li>
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<a href="/Team:Freiburg/Team/Sponsors">Sponsors</a></li><li>
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<a href="/Team:Freiburg/Team/Collaboration">Collaboration</a></li><li>
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<a href="/Team:Freiburg/Team/Pictures">Pictures</a></li>
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                <li><a href="/Team:Freiburg/Team/Judging">Judging</a></li>
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Revision as of 16:30, 8 October 2014

The AcCELLerator

Team

Members

We succeed to stably integrate our gene of interest into the genome of target cells by using a viral vector derived from the murine leukemia virus. The advantages of this vector are: its specificity for murine cells, making the viral work safe and easy; a very high efficiency for infection; and the ability of stable gene transfer into the genomes of target cells. Here we present results on these three qualities of our viral vector and how we optimized virus production and cell infection.

Team

Retrieved from "http://2014.igem.org/Team:Freiburg/Content/Team/Members"