Team:Warsaw/Calendar-Main/16 June 2008
From 2008.igem.org
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primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).<br> | primers (20 cycles, elongation duration 30 s, annealing temperature 58°C).<br> | ||
As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li> | As a result we got three PCR products: OmpA_linker and two fragments of TEM1 beta-lactamese: linker_alpha and linker_omega. </li> | ||
- | <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 proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).</li> | + | <li> Gel electrophoresis of PCR products (<a href="https://2008.igem.org/wiki/index.php?title=Team:Warsaw/Calendar-Main/16_June_2008#fig1">Fig. 1</a>) and <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#DNA_isolation_from_agarose_gel">gel-out</a> of proper bands (OmpA_linker - 500 bp, linker_alpha - 600 bp and linker_omega - 350 bp).</li> |
<li>Electrophoresis to estimate the concentration of isolated DNA.</li> | <li>Electrophoresis to estimate the concentration of isolated DNA.</li> | ||
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<li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol> | <li>Sequencing of proper fragments using primer <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#pZCseqL">pZCseqL</a>.</li></ol> | ||
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+ | <a name="fig1"><img src="https://static.igem.org/mediawiki/2008/a/a3/PCR_Ompa_Alpha_Omega_WAW.jpg" width=300/></a> | ||
+ | <var>PCR products: linker_alpha (lane 2), linker_omega (lane 3), OmpA_linker (lane 4)</var> | ||
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Revision as of 00:31, 12 October 2008
Preparation of constructs with OmpA protein fusionsMichał K.
Blue/white and rifampicin testMichał L., Ewa, Marcin
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