Team:Warsaw/Calendar-Main/15 July 2008
From 2008.igem.org
(Difference between revisions)
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<h3> Preparation of alpha+A conctruct</h3><h4>Antoni</h4> | <h3> Preparation of alpha+A conctruct</h3><h4>Antoni</h4> | ||
- | <p><ol><li>Gradient PCR on alpha+A PCR products with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a> primers.</li> | + | <p><ol><li>Gradient <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> on alpha+A PCR products with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AlphaL+SacI">AlphaL+SacI</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#AP+NotI">AP+NotI</a> primers.</li> |
<li>Gel electrophoresis. Again without satisfying results. | <li>Gel electrophoresis. Again without satisfying results. | ||
- | <li>Third PCR 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></ol></p> | </li></ol></p> | ||
Revision as of 00:10, 25 October 2008
Cloning of protein Z DNA to OmpA constructsMichał K.Two colonies (pACYC177+OmpA_Z_omega) was inoculated to liquid LB with kanamycin. Preparation of alpha+A conctructAntoni
Polymerase Chain Ligation on linker-A and omega-linkerMichał L., Ewa, Marcin
Fig. 1.Gradient PCR on alpha+A products. Lanes 1-3, 5, 6 - annealing temperature 68°C and DMSO concentration of 2%, 4%, 6%, 8% and 10% respectively. Lanes 7-11 - 72°C and DMSO concentration increasing in the same maner. Lane 4 and 12 GeneRuler DNA Ladder Mix 1 μg and 0.5 μg respectively. |