Team:Warsaw/Calendar-Stage2/21 September 2010

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<p align="justify">Six colonies were picked for inoculation of liquid cultures (three with B0032 and three with B0034). Cultures were grown for 6 h in 37 <sup>o</sup>C. Plasmids were purified with Plasmid Mini kit (A&amp;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>  
<p align="justify">Six colonies were picked for inoculation of liquid cultures (three with B0032 and three with B0034). Cultures were grown for 6 h in 37 <sup>o</sup>C. Plasmids were purified with Plasmid Mini kit (A&amp;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 src="https://static.igem.org/mediawiki/2010/e/e3/Minc1.jpg" height=400 width=400>
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<img src="https://static.igem.org/mediawiki/2010/e/e3/Minc1.jpg" height=400 width=500>
<p align="left"><i> M - size marker; 32a,b,c - plasmids harboring MinC under weak RBS; 34a,b,c - plasmids harboring MinC under strong RBS</i></p>
<p align="left"><i> M - size marker; 32a,b,c - plasmids harboring MinC under weak RBS; 34a,b,c - plasmids harboring MinC under strong RBS</i></p>
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<p align="justify">Samples 32a,b&c ans well as 34b&c appear to contain a correct construct. Smaller amounts of DNA obtained from B0034 may indicate a slight leaking of the construct (probably due to a read-through from the resistance gene).</p>
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<p align="justify">Samples 32a,b&c ans well as 34b&c appear to contain a correct construct. Smaller amounts of DNA with B0034-containing constructs may indicate a slight leaking of the construct (probably due to a read-through from the resistance gene).</p>

Latest revision as of 21:17, 25 October 2010

Example Tabs

Purification of MinC expression vectors

Kuba

Six colonies were picked for inoculation of liquid cultures (three with B0032 and three with B0034). 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.


M - size marker; 32a,b,c - plasmids harboring MinC under weak RBS; 34a,b,c - plasmids harboring MinC under strong RBS


Samples 32a,b&c ans well as 34b&c appear to contain a correct construct. Smaller amounts of DNA with B0034-containing constructs may indicate a slight leaking of the construct (probably due to a read-through from the resistance gene).