Team:Warsaw/Calendar-Main/11 July 2008
From 2008.igem.org
(Difference between revisions)
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<h3>Preparation of constructs with OmpA protein fusions</h3> | <h3>Preparation of constructs with OmpA protein fusions</h3> | ||
<p><ol> | <p><ol> | ||
- | <li> Colony PCR on colonies from plates with transformations OmpA_alpha. </li> | + | <li> Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on colonies from plates with transformations OmpA_alpha. </li> |
<li> Confirmed transformant colonies inoculated to liquid LB with kanamycin.</li> | <li> Confirmed transformant colonies inoculated to liquid LB with kanamycin.</li> | ||
</ol></p> | </ol></p> | ||
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<h3>Preparation of construct omega-A</h3> | <h3>Preparation of construct omega-A</h3> | ||
<p><ol> | <p><ol> | ||
- | <li> PCR A in 50 µl<br> | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> A in 50 µl<br> |
template DNA - pKS-A4 1 µl<br> | template DNA - pKS-A4 1 µl<br> | ||
primer <html> | primer <html> | ||
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<li>keeping in 4°C</li></ol> | <li>keeping in 4°C</li></ol> | ||
</li> | </li> | ||
- | <li> PCR omega in 50 µl<br> | + | <li> <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> omega in 50 µl<br> |
template DNA - pUC19 1 µl<br> | template DNA - pUC19 1 µl<br> | ||
primer OmegaLS - 2 µl<br> | primer OmegaLS - 2 µl<br> | ||
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<li> Gel electrophoresis</li> | <li> Gel electrophoresis</li> | ||
- | <li>Reisolation from agarose gel</li> | + | <li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Reisolation</a> from agarose gel</li> |
</ol> | </ol> | ||
</p> | </p> |
Revision as of 16:45, 5 October 2008
Preparation of constructs with OmpA protein fusions
Cloning of protein Z DNA to OmpA constructs2 colonies was inoculated to liquid LB broth with kanamycin Preparation of construct omega-A
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