Team:Warsaw/Calendar-Stage2/17 September 2010
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- | <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> |
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- | <img | + | <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
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.