Team:Warsaw/Calendar-Main/29 September 2008
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- | <h3>Preparation of | + | <h3>Preparation of pLac_OmpA_omega</h3> |
<h4>Michał K.</h4> | <h4>Michał K.</h4> | ||
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- | <li> Gel electrophoresis of PCR products <a href="https://2008.igem.org/Team:Warsaw/ | + | <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 band (pLac_OmpA_omega_ - 1200 bp)(<a href="https://2008.igem.org/Team:Warsaw/Calendar-Main/29_September_2008#fig1">Fig. 1.</a>).</li> |
</ol> | </ol> |
Revision as of 10:29, 27 October 2008
MutD5 testingPiotrSequencing results: there weren't any mutations in plasmids isolated from MutD5 - maybe this strain is too weak as a mutator. Preparation of pACYC177 + OmpA-linker-omega-linker (BBa_K103016)Michał K.
Preparation of pSB1A3+OmpA-linker (BBa_K103006)Michał K.
Preparation of pT7_omega_linkMichał K.
Preparation of pSB1A3+Z(BBa_K103004)Michał K.
Preparation of pLac_OmpA_omegaMichał K.
Preparation of vectors for BiobricksPiotrInoculation of bacteria received from iGEM HQs, carrying pSB2K3 and BBa_I739204 (pACYC177 converted into BioBrick vector) plasmids. Fig. 1. PCR on pLac_OmpA_omega_1. Marker 2. PCR product
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