Team:HokkaidoU Japan/Projects/asB0034/Method
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Revision as of 09:14, 14 October 2014
How to synthesize anti-sense RNA
Anti-sense RBS fragments were synthesized based on BioBrick by primer annealing. The sides of antisense fragment have scar and restriction enzymes XhoI, NcoI.
Fig1. How to make anti-sense B0034 by primer annealing
Fig2. Using restriction enzyme, XhoI, NcoI, we made stem_anti-sense conplex.
Fig3. Blue; antisense B0034, B0032 Red; scar sequence Green; NcoI site Purple; XhoI site
Fig4. Our parts
How to assay
we selected RFP and GFP for target genes. We used fluorophotometer to measure how anti-sense worked. The colonies transformed anti-sense RNA and target gene used to do assay.
(1)To cultivate the colony in 4 mL LB culture for about 20 hours
(2)To control turbidity up to 0.1 at OD600
(3)To cultivate the colony in 2 mL M9ZB culture for 9 hours (IPTG induces antisense RNA, addition 20 uL )
(4)To measure fluorescence after 9 hour
Fig4. Anti-sense B0034 is induced by IPTG