Team:Warsaw/Calendar-Main/17 June 2008
From 2008.igem.org
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primers (20 cycles, elongation length 1 min 15 s, annealing temperature 57°C).</li> | primers (20 cycles, elongation length 1 min 15 s, annealing temperature 57°C).</li> | ||
<li> Gel electrophoresis of PCR products and | <li> Gel electrophoresis of PCR products and | ||
- | <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of OmpA_alpha ( | + | <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of OmpA_alpha (1000 bp) and OmpA_omega (800 bp). </li> |
<li>Electrophoresis to estimate the concentration of isolated DNA.</li> | <li>Electrophoresis to estimate the concentration of isolated DNA.</li> | ||
<li> Overnight <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of purified OmpA_alpha and OmpA_omega DNA with NdeI and BamHI (Tango 2x buffer). </li> | <li> Overnight <a href="https://2008.igem.org/Wiki/Team:Warsaw/igem_notebook.htm#digest">digest</a> of purified OmpA_alpha and OmpA_omega DNA with NdeI and BamHI (Tango 2x buffer). </li> |
Revision as of 14:23, 11 October 2008
Preparation of constructs with OmpA protein fusionsMichał K.
Blue/white and rifampicin testMichał L., Ewa, MarcinRepetition of experiment from 11/06/2008.
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