Team:UPO-Sevilla/Notebook/08 03

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       <h2>Production Team</h2>
       <h2>Production Team</h2>
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       <p><strong>Paola Gallardo.</strong> We digest <i>fecI-fecR</i> with restriction enzymes PstI and EcoRI, and run an electrophoresis. We purified from electrophoresis gel (1'5 pDC) and ligate it with the vector C3L (chloramphenicol).</p>
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       <p>We digest <i>fecI-fecR</i> with PstI and EcoRI restriction enzymes , and run an electrophoresis. We purified from electrophoresis gel (1'5 pb) and ligate it with the vector C3L (chloramphenicol).</p>
       <h2>Assembly Team</h2>
       <h2>Assembly Team</h2>
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       <p>Again colony PCR of six candidates: 2+4, 2+5 y 2+7. We have positive candidates of UPO2+4 and UPO2+5. We set up inocula of this candidates and spread in LB+Tc plates.</p>
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       <p>We analyzed several candidates from 2+4, 2+5 and 2+7 plates by colony PCR. We had positive candidates of UPO2+4 and UPO2+5. We set up inocula of these candidates and spread on LB+Tc plates.</p>
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Latest revision as of 14:45, 27 October 2010

August, 3rd

Production Team

We digest fecI-fecR with PstI and EcoRI restriction enzymes , and run an electrophoresis. We purified from electrophoresis gel (1'5 pb) and ligate it with the vector C3L (chloramphenicol).

Assembly Team

We analyzed several candidates from 2+4, 2+5 and 2+7 plates by colony PCR. We had positive candidates of UPO2+4 and UPO2+5. We set up inocula of these candidates and spread on LB+Tc plates.

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