Team:Warsaw/Calendar-Main/27 June 2008

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<h4>Michał L., Ewa, Marcin</h4>
<h4>Michał L., Ewa, Marcin</h4>
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<li>Gel electophoresis of PCL products.</li>
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<li>Gel electophoresis of PCL products (Fig. 1.).</li>
<li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Gel-out</a> of proper bands (alpha-A: 1500 bp and omega-A: 1440 bp).</li>
<li><a href="https://2008.igem.org/Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Gel-out</a> of proper bands (alpha-A: 1500 bp and omega-A: 1440 bp).</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">Restriction digest</a> of pKS vector and the PCL products with NotI and SacI (BamHI buffer) for 2 hours.</li>
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest">Restriction digest</a> of pKS vector and the PCL products with NotI and SacI (BamHI buffer) for 2 hours.</li>
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<img src="https://static.igem.org/mediawiki/2008/e/ea/PCL_OmegaA_WAW.jpg" width=200/>
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<var><b>Fig. 1.</b>PCL product - Omega-A fusion.</var>
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Revision as of 11:16, 12 October 2008

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Preparation of constructs with OmpA protein fusions

Michał K.

Clean-up of OmpA_alpha and OmpA_omega digest products.

Cloning PCL products on pKS

Michał L., Ewa, Marcin

  1. Gel electophoresis of PCL products (Fig. 1.).
  2. Gel-out of proper bands (alpha-A: 1500 bp and omega-A: 1440 bp).
  3. Restriction digest of pKS vector and the PCL products with NotI and SacI (BamHI buffer) for 2 hours.
  4. Ligation 1 hour.
  5. Transformation of Top10 strain and screening on Amp100 plates.
Fig. 1.PCL product - Omega-A fusion.