Today we digested all our 4 new biobrick parts with both enzymes: ''Xba''I and ''Spe''I (Promoter of JEN1 from ''K. lactis''; Promoter of DLD1 from ''K. lactis''; Lysozyme from ''G. gallus''; Gene JEN1 from ''K. lactis''). We also digested the biofusion vector with the same enzymes for future ligation.
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*<p style=”text-align:justify;”>Today we digested all our 4 new biobrick parts with both enzymes: ''Xba''I and ''Spe''I (Promoter of JEN1 from ''K. lactis''; Promoter of DLD1 from ''K. lactis''; Lysozyme from ''G. gallus''; Gene JEN1 from ''K. lactis''). We also digested the biofusion vector with the same enzymes for future ligation.</p>
Once we confirmed the isolation of both finO and finP sequences from the R plasmid, we now proceed to the purification of the PCR's product. It's quite important to purify the reaction since it will be used for digestion and later ligation.
We purified both PCR's products by running an agarose gel of the entire product and then extracting the desirable band from the gel. We used Invitrogen's PureLink Quick Gel Extraction Kit to perform the purification, following the manufacturer's protocol without modifications (Protocol 7).
After the procedure, we ran an agarose gel with the resulting product in order to confirm purification. We purified both finO and finP!
Marcelo
Cre Recombinase
Today we performed minipreps of Cre-Recombinase´s biobrick, that we confirmed by running an electrophoresis agarose gel.
Víctor
YeastGuard
New biobricks
Today we digested all our 4 new biobrick parts with both enzymes: XbaI and SpeI (Promoter of JEN1 from K. lactis; Promoter of DLD1 from K. lactis; Lysozyme from G. gallus; Gene JEN1 from K. lactis). We also digested the biofusion vector with the same enzymes for future ligation.
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