Team:Warsaw/Calendar-Main/18 July 2008

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<li> Confirmed transformant colonies (found only on pACYC177+OmpA_A_alpha plate) inoculated to liquid LB with kanamycin. </li></ol>
<li> Confirmed transformant colonies (found only on pACYC177+OmpA_A_alpha plate) inoculated to liquid LB with kanamycin. </li></ol>
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<h3>Paweł</h3>
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<h3>Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA<br>
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Paweł</h3>
<p><ol><li>Ligation transformed into TOP10 strain and plated on LB+kanamycin</li>
<p><ol><li>Ligation transformed into TOP10 strain and plated on LB+kanamycin</li>
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Revision as of 16:39, 2 October 2008

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Cloning of protein A DNA to OmpA constructs

  1. Colony PCR on colonies from plates with transformations pACYC177+OmpA_A_omega and pACYC177+OmpA_A_alpha. Primers used: AL+SacI and AP+NotI
  2. Confirmed transformant colonies (found only on pACYC177+OmpA_A_alpha plate) inoculated to liquid LB with kanamycin.

Cloning of protein Z DNA to pET15b-OmpA-omega in place of OmpA
Paweł

  1. Ligation transformed into TOP10 strain and plated on LB+kanamycin


Cloning of protein A DNA to pET15b+Omp-alfa plasmid
Antoni

  1. Isolation of plasmids from cultures inocluated on previous day (pGeneart+A and pET15b+OmpA-alfa).
  2. Digest pET15b+OmpA_alpha and pGeneart+A with NdeI and NotI, pET15b+OmpA_alpha dephosphorylation with CIAP
  3. Gel electrophoresis of digested plasmids and gel-out of proper bands
  4. Overnight ligation of pET15b+alfa and A