Team:Goettingen/week2-3

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Revision as of 19:40, 11 September 2012

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Amplification of tar gene

Experiment:
PCR was performed with isolated genomic DNA from DH10B, forward and reverse primers of tar and using Pfu polymerase.

Amplification of tar gene

Experiment:
PCR was controlled by running a 1% agarose gel. As standard, Gene Ruler 1kb ladder (ThermoScientific) was used. A band at about 1.6 kb was detected. Amplification of tar was successful.

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 <ul>
 <li>Experiment: <br>PCR was performed with isolated genomic DNA from DH10B, forward and reverse primers of <i>tar</i> and using <i>Pfu</i> polymerase.
+</li>
+</ul>
+<br></td></tr>
+</table>
+<br>
+<table cellpadding="20 px" border="1" bordercolor="black" valign="top">
+<tr bordercolor="black" valign="top">
+<td width="900" bordercolor="black" valign="top">
+<h2><b>V05_10 </b></h2><br>
+<b>Amplification of <i>tar</i> gene</b><br>
+<ul>
+<li>Experiment: <br>PCR was controlled by running a 1% agarose gel. As standard, Gene Ruler 1kb ladder (ThermoScientific) was used. A band at about 1.6 kb was detected. Amplification of <i>tar</i> was successful.
 </li>
 </ul>