Team:Warsaw/Calendar-Main/29 September 2008
From 2008.igem.org
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- | <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 ( | + | <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 (BBa_K103018 - 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 19:50, 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 OmpA-linker-omega-linker (BBa_K103016)Michał K.
Preparation of OmpA-linker (BBa_K103006)Michał K.
Preparation of omega_linker under PT7 (BBa_K103020)Michał K.
Preparation of Z(BBa_K103004)Michał K.
Preparation of OmpA_linker_omega_linker under Plac (BBa_K103018)Michał K.
1. Marker 2. PCR product Preparation of vectors for BiobricksPiotrInoculation of bacteria received from iGEM HQs, carrying pSB2K3 and BBa_I739204 (pACYC177 converted into BioBrick vector) plasmids.
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