Team:UNICAMP-Brazil/Notebooks/September 27
From 2009.igem.org
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*<p style=”text-align:justify;”>We don’t have time, the deadline is next. So, we decided just isolate both CeaB and CeiB in a plasmid backbone. We chose isolating into [http://partsregistry.org/Part:pSB1A3 pSBA3] plasmid. Thus, we digested the plasmid with the right restriction enzymes (SpeI and XbaI). Immediately, we made the purification gel according to the [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Purification_of_DNA_fragments_from_agarose_gels protocol 7].</p> | *<p style=”text-align:justify;”>We don’t have time, the deadline is next. So, we decided just isolate both CeaB and CeiB in a plasmid backbone. We chose isolating into [http://partsregistry.org/Part:pSB1A3 pSBA3] plasmid. Thus, we digested the plasmid with the right restriction enzymes (SpeI and XbaI). Immediately, we made the purification gel according to the [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Purification_of_DNA_fragments_from_agarose_gels protocol 7].</p> | ||
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''Luige'' | ''Luige'' | ||
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+ | ====Cre-Recombinase - New PCR==== | ||
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+ | * After several attempts on correctly digesting Cre-Recombinase's fragment, we ended up without any sample! =/ | ||
+ | * Therefore, today we repeated the PCR reaction for amplifying Cre-Recombinase without ATG, in order to generate more sample. | ||
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+ | ''Víctor'' | ||
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==''' YeastGuard '''== | ==''' YeastGuard '''== | ||
Revision as of 18:41, 21 October 2009
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