Team:HokkaidoU Japan/Projects/Length/Method
From 2014.igem.org
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- | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem">H- | + | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem">H-stem System</a></li> |
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem#Overview">Overview</a></li> | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem#Overview">Overview</a></li> | ||
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem#How_To_Use">How To Use</a></li> | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem#How_To_Use">How To Use</a></li> | ||
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- | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Overview">Anti- | + | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Overview">Anti-sense B0034</a></li> |
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Overview">Overview</a></li> | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Overview">Overview</a></li> | ||
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Method">Method</a></li> | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Method">Method</a></li> |
Revision as of 12:00, 14 October 2014
How to synthesize anti-sense constructs
Anti-sense fragments were synthesized based on BioBrick by PCR. Forward primers are common. Each reverse primers are different. Because of these, we got various length anti-senses. The sides of antisense fragment have restriction enzymes XhoI, NcoI sites. We finished synthesizing anti-sense RNA, we ligated each anti-senses with H-stem vector by restriction enzyme XhoI, NcoI.
Therefore, we got as90, as120. As the same way, we made as30, as60 in H-Stem System and Anti-sense B0034 examination. We performed repression examination by using their 4 anti-sense constructs.
How to assay
We selected mRFP for the target gene. We used fluorophotometer to measure how anti-sense worked. The colonies transformed by anti-sense constructs and target gene was used for assay.
- To cultivate the colony in 4 mL LB culture for about 20 hours
- To control turbidity up to 0.1 at OD600
- To cultivate the colony in 2 mL M9ZB culture for 9 hours (100mM IPTG induces antisense constructs, addition 20 uL)
- To measure fluorescence after 9 hour