Team:UNICAMP-Brazil/Notebooks/September 27
From 2009.igem.org
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====Digestion of pTet and Double Terminator==== | ====Digestion of pTet and Double Terminator==== | ||
- | *<p style=”text-align:justify;”>We | + | *<p style=”text-align:justify;”>We intend to ligate the parts which we are recovering right now (started yesterday) onto biobricks BBa_R0040 (pTet) and BBa_B0015 (double terminator), using it's own vector.</p> |
*<p style=”text-align:justify;”>Those biobricks were already recovered on August 10th.</p> | *<p style=”text-align:justify;”>Those biobricks were already recovered on August 10th.</p> | ||
- | *<p style=”text-align:justify;”>BBa_R0040 was digested with | + | *<p style=”text-align:justify;”>BBa_R0040 was digested with ''Spe''I and ''Pst''I, once we intend to add a fragment in front of it (downstream). As for BBa_B0015, the digestion was realized with ''EcoR''I and ''Xba''I restriction enzymes, once we need to insert a fragment behind it's part (upstream).</p> |
*<p style=”text-align:justify;”>Digestion lasted 3 hours.</p> | *<p style=”text-align:justify;”>Digestion lasted 3 hours.</p> | ||
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====CeaB and CeiB==== | ====CeaB and CeiB==== | ||
- | *<p style=”text-align:justify;”>We don’t have time, the deadline is | + | *<p style=”text-align:justify;”>We don’t have time, the deadline is near. So, we decided to just isolate both CeaB and CeiB in a plasmid backbone. We chose to isolate into [http://partsregistry.org/Part:pSB1A3 pSBA3] plasmid. Thus, we digested the plasmid with the right appropriate enzymes (''Spe''I and ''Xba''I). Immediately, we made the purification gel according to [https://2009.igem.org/Team:UNICAMP-Brazil/Protocols/Purification_of_DNA_fragments_from_agarose_gels Protocol 7].</p> |
''Luige'' | ''Luige'' |
Latest revision as of 03:23, 22 October 2009
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