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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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| - | One transformed colony seemed correct, the others were probably satellite colonies without the plasmid.<br/> | + | |
| + | <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/> | ||
Start of 5mL liquid culture of the main colony. <br/> | Start of 5mL liquid culture of the main colony. <br/> | ||
Plating of the satellite colonies to check the presence of the plasmid <br/> | Plating of the satellite colonies to check the presence of the plasmid <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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| - | Miniprep on the four clones. Verification of plasmid by digestion (EcoRI, HindIII) | + | |
| + | <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) | ||
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| - | 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) | + | |
| + | <FONT COLOR="green"> <b>PCR and mutagenesis of rcn, csgBA, csgEFG</b> </FONT> <br><br> | ||
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| + | <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> | ||
| + | <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)
