Team:Warsaw/Calendar-Main/23 June 2008

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<h4>Michał L., Ewa, Marcin:</h4>
<h4>Michał L., Ewa, Marcin:</h4>
<ol><li>We have successfully amplified Omega-linker, but were unable to obtain the other two. PCRs were repeated. New annealing temp.: 48&deg;C. Mg<sup>2+</sup> concentration elevated to 12 μM.</li></ol>
<ol><li>We have successfully amplified Omega-linker, but were unable to obtain the other two. PCRs were repeated. New annealing temp.: 48&deg;C. Mg<sup>2+</sup> concentration elevated to 12 μM.</li></ol>
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<h3>Preparation of constructs with OmpA protein fusions</h3>
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<h4>Michał K.:</h4>
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<ol>
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<li> Inoculation other separate transformant colonies from plates with ligations: pACYC177+OmpA_alpha pACYC177+OmpA_omega (liquid LB + kanamycin).</li>
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<li>
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<li> PCR on isolated plasmids with </ol>
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Contents

PCR results

Michał L., Ewa, Marcin:

  1. We have successfully amplified Omega-linker, but were unable to obtain the other two. PCRs were repeated. New annealing temp.: 48°C. Mg2+ concentration elevated to 12 μM.

Preparation of constructs with OmpA protein fusions

Michał K.:

  1. Inoculation other separate transformant colonies from plates with ligations: pACYC177+OmpA_alpha pACYC177+OmpA_omega (liquid LB + kanamycin).
  2. PCR on isolated plasmids with