Team:Warsaw/Calendar-Main/24 June 2008
From 2008.igem.org
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<p>Still no success. We need to run gradient PCR to find optimal reaction conditions.</p> | <p>Still no success. We need to run gradient PCR to find optimal reaction conditions.</p> | ||
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+ | <h3>Cloning of protein Z DNA to <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2BOmpA-alpha>pET15b-OmpA-alpha</a> in place of OmpA</h3> | ||
+ | <h4>Paweł</h4> | ||
+ | <p><ol> | ||
+ | <li>Control <a href=https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#digest>digest</a> of isolated plasmids with NdeI and NotI. Two positives obtained (proper band: ~200 bp visible).</li> | ||
+ | <li>One of positive plasmids transformed into <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#top10">TOP10</a> and plated on LB+amp, overnight, for further isolation of <a href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pET15b%2Bhis%2BZ%2Bomega>pET15b+Z+omega</a> vector.</li> | ||
+ | </ol></p> | ||
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<li>Gel electrophoresis (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/24_June_2008#fig1">Fig. 1</a>, no proper clones found).</li> | <li>Gel electrophoresis (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/24_June_2008#fig1">Fig. 1</a>, no proper clones found).</li> | ||
</ol> | </ol> | ||
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Revision as of 20:17, 19 October 2008
Preparation of alpha-A and omega-A fusionsMichał L., Ewa, MarcinStill no success. We need to run gradient PCR to find optimal reaction conditions. Cloning of protein Z DNA to pET15b-OmpA-alpha in place of OmpAPaweł
Preparation of constructs with OmpA protein fusionsMichał K.
Fig. 1. PCR product - searching for fusions with OmpA protein. Lower lanes - OmpA_alpha, upper - OmpA_omega.
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