Team:Warsaw/Calendar-Main/15 July 2008
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<h3>Cloning of protein Z DNA to OmpA constructs</h3><h4>Michał K.</h4> | <h3>Cloning of protein Z DNA to OmpA constructs</h3><h4>Michał K.</h4> | ||
- | <p> Two colonies (<A href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a>) | + | <p> Two colonies (<A href=https://2008.igem.org/Wiki/Team:Warsaw/vectors/pACYC177%2BompA-Z-omega>pACYC177+OmpA_Z_omega</a>) were inoculated to liquid LB with kanamycin.</p> |
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<li>Gel electrophoresis. Again without satisfying results. | <li>Gel electrophoresis. Again without satisfying results. | ||
<li>Third <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on alpha+A. This time two temperatures of annealing (68°C and 72°C) and gradient of DMSO.</li> | <li>Third <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on alpha+A. This time two temperatures of annealing (68°C and 72°C) and gradient of DMSO.</li> | ||
- | <li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/15_July_2008#fig1">Fig. 1</a>). | + | <li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/15_July_2008#fig1">Fig. 1.</a>). |
<li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Gel-out</a> of proper 1000 bp band.</li> | <li><a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">Gel-out</a> of proper 1000 bp band.</li> | ||
</li></ol></p> | </li></ol></p> |
Latest revision as of 17:59, 26 October 2008
Cloning of protein Z DNA to OmpA constructsMichał K.Two colonies (pACYC177+OmpA_Z_omega) were inoculated to liquid LB with kanamycin. Cloning omega-A fusion on pKS (second attempt)Michał L., Ewa, MarcinPolymerase Chain Ligation on linker-A and omega-linker
Preparation of alpha+A conctructAntoni
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