From 2008.igem.org
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- | <h3> Preparation of alpha+A conctruct</h3><h4>Antoni</h4>
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- | <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>
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- | <li>Gel electrophoresis. Again without satisfying results.
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- | <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>
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- | <li>Gel electrophoresis (<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/15_July_2008#fig1">Fig. 1</a>).
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- | <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>
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- | </li></ol></p>
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Revision as of 17:47, 26 October 2008
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Cloning of protein Z DNA to OmpA constructsMichał K.
Two colonies (pACYC177+OmpA_Z_omega) was inoculated to liquid LB with kanamycin.
Cloning omega-A fusion on pKS (second attempt)
Michał L., Ewa, Marcin
Polymerase Chain Ligation on linker-A and omega-linker
- reisolated PCR product omega-linker - 4 µl
- reisolated PCR product linker-A - 13.5 µl
- primer
OmegaL+SacI - 2 µl
- primer
AP+NotI - 2 µl
- Pfu buffer with Mg2+ - 5 µl
- dNTPs - 1 µl
- H2o - 22 µl
- Program:
- 95°C - 3'
- 95°C - 30"
- 55°C - 45"
- 68°C - 1'
- go to step 2 25 x
- 68° - 10'
- keep in 4°
- gel electrophoresis of products
Preparation of alpha+A conctructAntoni
- Gradient PCR on alpha+A PCR products with AlphaL+SacI and AP+NotI primers.
- Gel electrophoresis. Again without satisfying results.
- Third PCR on alpha+A. This time two temperatures of annealing (68°C and 72°C) and gradient of DMSO.
- Gel electrophoresis (Fig. 1).
- Gel-out of proper 1000 bp band.
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.
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