Team:Lyon-INSA-ENS/Realisation/Week2

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     <h1 style="color: white;"> Week 2 </h1>     
     <h1 style="color: white;"> Week 2 </h1>     
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<FONT COLOR="orange"> <b> Extraction of NiCoT </b></FONT> <br><br>
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One transformed colony (NicoT in NM522) seemed correct, the others were probably satellite colonies without the plasmid.<br/>
One transformed colony (NicoT in NM522) seemed correct, the others were probably satellite colonies without the plasmid.<br/>
Start of 5mL liquid culture of the main colony. <br/>
Start of 5mL liquid culture of the main colony. <br/>
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<FONT COLOR="orange"> <b> Extraction of NiCoT </b></FONT> <br><br>
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4 more new clones have grown : start of 5mL liquid cultures on these clones.
4 more new clones have grown : start of 5mL liquid cultures on these clones.
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<FONT COLOR="orange"> <b> Extraction of NiCoT </b></FONT> <br><br>
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Miniprep on the four clones. Verification of plasmid by <b>digestion</b> (EcoRI, HindIII)
Miniprep on the four clones. Verification of plasmid by <b>digestion</b> (EcoRI, HindIII)
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<FONT COLOR="green"> <b>PCR and mutagenesis of rcn, csgBA, csgBAEFG</b> </FONT> <br><br>
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<FONT COLOR="green"> <b>PCR and mutagenesis of rcn, csgBA, csgEFG</b> </FONT> <br><br>
<b>PCR</b> from genomic DNA from E.coli strain MC4100 to amplify three genes : RcnR (cobalt receptor), CsgAB (curli operon, part 1) and CsgEFG (curli operon, part 2)
<b>PCR</b> from genomic DNA from E.coli strain MC4100 to amplify three genes : RcnR (cobalt receptor), CsgAB (curli operon, part 1) and CsgEFG (curli operon, part 2)
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              <a  href="https://2011.igem.org/Team:Lyon-INSA-ENS/Realisation/Week2"/><font color="grey"><b>Previous Week</b></font></a>
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              <a  style = "float : right"; href="https://2011.igem.org/Team:Lyon-INSA-ENS/Realisation/Week3"/><font color="grey"><b>Next Week</b></font></a>
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Latest revision as of 23:34, 21 September 2011







Week 2


From Monday the 20th of June to Friday the 24th of June 2011





Monday


Extraction of NiCoT

One transformed colony (NicoT in NM522) seemed correct, the others were probably satellite colonies without the plasmid.
Start of 5mL liquid culture of the main colony.
Plating of the satellite colonies to check the presence of the plasmid





Tuesday


Extraction of NiCoT

4 more new clones have grown : start of 5mL liquid cultures on these clones.





Wednesday


Extraction of NiCoT

Miniprep on the four clones. Verification of plasmid by digestion (EcoRI, HindIII)





Thursday


PCR and mutagenesis of rcn, csgBA, csgEFG

PCR from genomic DNA from E.coli strain MC4100 to amplify three genes : RcnR (cobalt receptor), CsgAB (curli operon, part 1) and CsgEFG (curli operon, part 2)













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ENS assystem Biomérieux INSA INSA