Team:HokkaidoU Japan/Projects/asB0034/Method
From 2014.igem.org
(Difference between revisions)
Kakurehana (Talk | contribs) |
Kakurehana (Talk | contribs) |
||
Line 118: | Line 118: | ||
<div class="fig fig800"> | <div class="fig fig800"> | ||
<img src="https://static.igem.org/mediawiki/2014/2/25/HokkaidoU_antisenseB0034_overview09.png"> | <img src="https://static.igem.org/mediawiki/2014/2/25/HokkaidoU_antisenseB0034_overview09.png"> | ||
- | <div>Antisense B0034 is induce by IPTG</div> | + | <div>Fig3. Antisense B0034 is induce by IPTG</div> |
</div> | </div> | ||
Revision as of 08:00, 14 October 2014
How to synthesize antisense RNA
Antisense-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 antisense B0034 by primer annealing
Fig2. Using restriction enzyme, XhoI, NcoI, we made stem-antisense conplex.
How to assay
we selected RFP and GFP for target genes. We used fluorophotometer to measure how antisense worked. The colonies transformed antisense 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
Fig3. Antisense B0034 is induce by IPTG