Team:Goettingen/week2-2

From 2012.igem.org

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<h2><b>V05_10</b></h2><br>
<h2><b>V05_10</b></h2><br>
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<b>Purificaton of <i>flhDC</i> </b></b></h2><br>
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<b>Separation of <i>flhDC</i> </b></b></h2><br>
<ul>
<ul>
<li>Experiment: <br>  The amplicon was analsed and separated via application on an 1% agarose gel. As standard, Gene Ruler 1kb ladder (ThermoScientific) was used. The gel featured a clear band at about 900 kb. The amplification of <i>flhDC</i> was successful. </li>
<li>Experiment: <br>  The amplicon was analsed and separated via application on an 1% agarose gel. As standard, Gene Ruler 1kb ladder (ThermoScientific) was used. The gel featured a clear band at about 900 kb. The amplification of <i>flhDC</i> was successful. </li>
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<br> </li>
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</ul>
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<br></td></tr>
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</table>
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<br>
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<h2><b>V05_11</b></h2><br>
 +
<b>Purificaton of <i>flhDC</i> </b></b></h2><br>
 +
<ul>
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<li>Experiment: <br>  The PCR-product was purified using peqGOLD Gel Extraction Kit (Peqlab) according to the manual. </li>
<br> </li>
<br> </li>
</ul>
</ul>

Revision as of 20:46, 13 September 2012

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