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Team:Heidelberg/testing/Frontpage
From 2014.igem.org
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| - | <h1 style="text-align: right; color: | + | <h1 style="text-align: right; color: black;" ><span style="font-size: 0.8em;">circular <span style="color:white;">heat-stable</span></span><br>Xylanase</h1> |
<p>Wouldn´t it be great to amplify DNA in a normal PCR maintaining the epigenetic information coded in methylation patterns?</p> | <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. | <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. | ||
Revision as of 10:21, 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.
circular heat-stable
Xylanase
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.
