Team:HokkaidoU Japan/Projects/Length/Method
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<h1> How to synthesize anti-sense constructs</h1> | <h1> How to synthesize anti-sense constructs</h1> | ||
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- | Anti-sense fragments were synthesized based on BioBrick by PCR. Forward primers are common (XhoI-Ptet (-10)). Each reverse primers are different (as90 NcoI, as120 NcoI) (Fig. 1). Because of these, we got various length anti-senses. The sides of antisense fragment have restriction enzymes XhoI, NcoI sites. | + | Anti-sense fragments were synthesized based on BioBrick by PCR. Forward primers are common (XhoI-Ptet (-10)). Each reverse primers are different (as90 NcoI, as120 NcoI) (Fig. 1). As90 is the anti-sense that covers 90 bp of mRNA, and as 120 is the anti-sense that covers 120 bp of mRNA (complement RBS and a part of mRFP sequence.) Because of these, we got various length anti-senses. The sides of antisense fragment have restriction enzymes XhoI, NcoI sites. After we finished synthesizing anti-sense fragments, we cut and ligated each anti-senses with H-stem vector.</p> |
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<p> | <p> | ||
- | Therefore, we got | + | Therefore, we got anti-sense fragment, as90 and 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.</p> |
<h1><p>How to assay</p> | <h1><p>How to assay</p> |
Revision as of 14:00, 14 October 2014
How to synthesize anti-sense constructs
Anti-sense fragments were synthesized based on BioBrick by PCR. Forward primers are common (XhoI-Ptet (-10)). Each reverse primers are different (as90 NcoI, as120 NcoI) (Fig. 1). As90 is the anti-sense that covers 90 bp of mRNA, and as 120 is the anti-sense that covers 120 bp of mRNA (complement RBS and a part of mRFP sequence.) Because of these, we got various length anti-senses. The sides of antisense fragment have restriction enzymes XhoI, NcoI sites. After we finished synthesizing anti-sense fragments, we cut and ligated each anti-senses with H-stem vector.
Therefore, we got anti-sense fragment, as90 and 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