Team:Warsaw/Calendar-Main/15 July 2008
From 2008.igem.org
(Difference between revisions)
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<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 PCR on alpha+A. This time two temperatures of annealing (68°C and 72°C) and gradient of DMSO</li> | ||
- | <li>Gel electrophoresis. | + | <li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/15_July_2008#fig1>fig. 1.</a> |
</li></ol></p> | </li></ol></p> | ||
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</p> | </p> | ||
- | + | <br> | |
- | + | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/c/c5/PCRalfa%2BAzDMSO.jpg"></a> | |
+ | <var><b>Fig. 1.</b>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. | ||
Revision as of 23:58, 24 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
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. |