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Team:Heidelberg/testing/Frontpage
From 2014.igem.org
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<div style="position:relative;" class="row"> | <div style="position:relative;" class="row"> | ||
<div class="jumbotron slide grey"> | <div class="jumbotron slide grey"> | ||
| - | + | <div> | |
| - | + | <div class="col-lg-4 col-lg-push-8" style="z-index:5;"> | |
| - | + | <img class="img-responsive" src="/wiki/images/a/a6/Heidelberg_Project_Dnmt1.png" /> | |
| - | + | </div> | |
| - | + | <div class="col-lg-8 col-lg-pull-4"> | |
| - | + | <h1 class="dark-grey-text" style="text-align: right;"><span style="font-size: 0.8em;">circular <span class="red-text">heat-stable</span></span><br>DNMT1</h1> | |
| - | + | <p>Wouldn´t it be great to amplify DNA in a normal PCR maintaining the epigenetic information coded in methylation patterns?</p> | |
| - | + | <p>The problem: DNMT I, an enzyme which is responsible for the establishment and maintenance of the individual methylation pattern of different cell types, is not heat stable. | |
| - | + | For iGEM 2014 we therefore create a PCR 2.0 with heat-stable DNMT I by circularization. | |
| - | + | </p> | |
| - | + | </div> | |
| - | + | <div class="clearfix"></div> | |
| - | + | </div> | |
| - | + | <div class="title-wrapper-dnmt1" style="color:white;"> | |
<span class="title-dnmt1">PCR 2.0</span> | <span class="title-dnmt1">PCR 2.0</span> | ||
<span class="special-span-dnmt1"></span> | <span class="special-span-dnmt1"></span> | ||
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</div> | </div> | ||
</div> | </div> | ||
<div style="position:relative;" class="row"> | <div style="position:relative;" class="row"> | ||
<div class="jumbotron slide red"> | <div class="jumbotron slide red"> | ||
| - | + | <div> | |
| - | + | <div class="col-lg-4" style="z-index:5;"> | |
| - | + | <img class="img-responsive" src="/wiki/images/8/82/Heidelberg_Project_Xylanase.png" /> | |
| - | + | <div style="height: 80px;" class="hidden-sm hidden-xs"></div> | |
| - | + | </div> | |
| - | + | <div class="col-lg-8"> | |
| - | + | <h1 style="text-align: right; color: black; padding-right: 130px;" ><span style="font-size: 0.8em;">circular <span style="color:white;">heat-stable</span></span><br><span style="font-size:1.3em;">Xylanase</span></h1> | |
| - | + | <p>Xylanase is an important enzyme for the pulp and paper industry.</p> | |
| - | + | <p>Bla bla</p> | |
| + | <p>In future Xylanase could be used for the production of biofuel.</p> | ||
| + | </div> | ||
| + | <div class="clearfix"></div> | ||
| + | </div> | ||
| + | <div class="title-wrapper-xylanase" style="text-align: right; color:white;"> | ||
| + | <span class="title-xylanase">INDUSTRY</span> | ||
| + | <span class="special-span-xylanase"></span> | ||
</div> | </div> | ||
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Revision as of 10:53, 9 October 2014
iGEM TEAM HEIDELBERG 2014
THE RING
OF FIRE
Dieser Text soll reinhauen.
Am besten sollte er richtig gut sein!
circular heat-stable
DNMT1
Wouldn´t it be great to amplify DNA in a normal PCR maintaining the epigenetic information coded in methylation patterns?
The problem: DNMT I, an enzyme which is responsible for the establishment and maintenance of the individual methylation pattern of different cell types, is not heat stable. For iGEM 2014 we therefore create a PCR 2.0 with heat-stable DNMT I by circularization.
PCR 2.0
circular heat-stable
Xylanase
Xylanase is an important enzyme for the pulp and paper industry.
Bla bla
In future Xylanase could be used for the production of biofuel.
INDUSTRY
