Team:Warsaw/Calendar-Stage2/17 September 2010

From 2010.igem.org

(Difference between revisions)
(New page: <html> <script type="text/javascript"> ActiveTab='WetLab'; </script> </html> {{TemplateTop}} {{UpperTabs}} {{LowerTabsTeam}} <html> <!-- do not edit above me! --> <h2>Mutagenesis of MinC<...)
Line 12: Line 12:
<h2>Mutagenesis of MinC</h2>
<h2>Mutagenesis of MinC</h2>
<h4>Kuba</h4>
<h4>Kuba</h4>
-
<p align="justify">Four colonies were picked for inoculation of liquid cultures. Cultures were grown for 6 h in 37 <sup>o</sup>C. Plasmids were purified with Plasmid Mini kit (A&A) biotechnology. The obtained sample, as well as the initial (unmutated) plasmid, were then digested with EcoRI and PstI for 1 h and run on agarose gel.  
+
<p align="justify">Four colonies were picked for inoculation of liquid cultures. Cultures were grown for 6 h in 37 <sup>o</sup>C. Plasmids were purified with Plasmid Mini kit (A&A) biotechnology. The obtained sample, as well as the initial (unmutated) plasmid, were then digested with EcoRI and PstI for 1 h and run on agarose gel.</p>
<br>
<br>
-
<img href="https://static.igem.org/mediawiki/2010/8/8f/Minc2_copy.jpg" height=200 width=200>
+
<img align="center" src="https://static.igem.org/mediawiki/2010/8/8f/Minc2_copy.jpg" height=200 width=200>
-
<i>C - unmutated plasmid; M - marker; 1,2,3,4 -respective samples</i>
+
<p align="center"><i>C - unmutated plasmid; M - marker; 1,2,3,4 -respective samples</i></p>
<br>
<br>
-
The shorter band in samples 1,2,3 appears to be slightly longer compared to control, indicating a succesfull mutagenesis. These conclusions were later verified by sequencing.</p>
+
<p align="justify">The shorter band in samples 1,2,3 appears to be slightly longer compared to control, indicating a succesfull mutagenesis. These conclusions were later verified by sequencing.</p>

Revision as of 15:32, 25 October 2010

Example Tabs

Mutagenesis of MinC

Kuba

Four colonies were picked for inoculation of liquid cultures. Cultures were grown for 6 h in 37 oC. Plasmids were purified with Plasmid Mini kit (A&A) biotechnology. The obtained sample, as well as the initial (unmutated) plasmid, were then digested with EcoRI and PstI for 1 h and run on agarose gel.


C - unmutated plasmid; M - marker; 1,2,3,4 -respective samples


The shorter band in samples 1,2,3 appears to be slightly longer compared to control, indicating a succesfull mutagenesis. These conclusions were later verified by sequencing.