Team:Goettingen/week20-2
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<li>Experiment: <br> MotA and MotB were digested with XbaI and PstI. The plasmids with the different promoters were treated with SpeI and PstI. Digestion was controlled via gel-electrophoresis.The expected bands were isolated from the gel and purified via PeqGOLD Gelextraction Kit (Peqlab).</li> | <li>Experiment: <br> MotA and MotB were digested with XbaI and PstI. The plasmids with the different promoters were treated with SpeI and PstI. Digestion was controlled via gel-electrophoresis.The expected bands were isolated from the gel and purified via PeqGOLD Gelextraction Kit (Peqlab).</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>V09_10_3 </b></h2><br> | ||
+ | <b>Quickchange of FliC</b><br> | ||
+ | <ul> | ||
+ | <li>Experiment: <br> Quick Change overlapping PCR was performed using designed primers and Pfu Turbo polymerase (see Quick Change protocol in "protocols").</li> | ||
</ul> | </ul> | ||
<br></td></tr> | <br></td></tr> |
Revision as of 12:01, 11 September 2012
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#2 Speed Improvement - 20th weekBack to overview
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