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− | <h1>RESULT</h1> | + | <h1><font color="#005EFF">RESULT</font></h1> |
− | <p> | + | <p>Construction of Cure allergic Rhinitis System</p> |
+ | <dl> | ||
+ | <dt>Plasmid 1</dt> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/8/8e/T--KAIT_JAPAN--plasmod1bp.png"height="100" width="650"></center></p> | ||
+ | <dd>IL-10Receptor, STAT1 and JAK are cloned to produce plasmid 1.</dd> | ||
+ | <dd>Figure below shows colonies observation images obtained by binding all genes, placing them in pSB1C3 and transforming them into DH5α.</dd> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/2/2e/T--KAIT_JAPAN--IL-10colony.png"height="600" width="650"></center></p> | ||
+ | <dd>Picture of agar gel electrophoresis result of plasmid extraction from the obtained colony is shown in figure below.</dd> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/f/f2/T--KAIT_JAPAN--IL-10_DNA.png"height="500" width="400"></center></p> | ||
+ | <dd>From figure above, we can confirm that the plasmid obtained is consistent with the molecular weight targeted.</dd> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | <dt>Plasmid 2</dt> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/d/d3/T--KAIT_JAPAN--plasmid2bp.png"height="100" width="650"></center></p> | ||
+ | <dd>              Total: about 7443bp</dd> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/6/62/T--KAIT_JAPAN--HlyA-IL-12.png"height="60" width="650"></center></p> | ||
+ | <br> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/9/9b/T--KAIT_JAPAN--GFP-HlyA.png"height="60" width="650"></center></p> | ||
+ | <br> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/6/67/T--KAIT_JAPAN--HlyA-GFP.png"height="60" width="650"></center></p> | ||
+ | <br> | ||
+ | <dd>In order to create plasmid 2 (4 patterns), GFAPpromoter, HlyD, HlyB, TolC, and HlyA + IL-12 or GFP were cloned.</dd> | ||
+ | <dd>This four plasmids has the same molecular weight.</dd> | ||
+ | <dd>The four figure below shows colony observation image obtained by binding all genes and inserts them in pSB1C3 and transforms them into DH5α.</dd> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/c/cc/T--KAIT_JAPAN--HlyA1colony.png"height="600" width="650"></center></p> | ||
+ | <br> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/c/c7/T--KAIT_JAPAN--HlyA2.png"height="600" width="650"></center></p><br> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/9/93/T--KAIT_JAPAN--HlyA3.png"height="600" width="650"></center></p><br> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/4/44/T--KAIT_JAPAN--HlyA4.png"height="600" width="650"></center></p> | ||
+ | <br> | ||
+ | <dd>Agarose gel electrophoresis result of plasmid extraction from the obtained colonies is shown in figure below.</dd> | ||
+ | <p><center><img src="https://static.igem.org/mediawiki/2017/1/15/T--KAIT_JAPAN--plasmiod2_DNA.png"height="500" width="400"></center></p> | ||
+ | <dd>From figure above, we can confirm that all the plasmids obtained are plasmid 2 since the molecular weight is consistent with the molecular weight targeted.</dd> | ||
+ | </dl> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | |||
</main> | </main> | ||
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{{KAIT_JAPAN_footer}} | {{KAIT_JAPAN_footer}} |
Latest revision as of 02:19, 2 November 2017
RESULT
Construction of Cure allergic Rhinitis System
- Plasmid 1
- IL-10Receptor, STAT1 and JAK are cloned to produce plasmid 1.
- Figure below shows colonies observation images obtained by binding all genes, placing them in pSB1C3 and transforming them into DH5α.
- Picture of agar gel electrophoresis result of plasmid extraction from the obtained colony is shown in figure below.
- From figure above, we can confirm that the plasmid obtained is consistent with the molecular weight targeted.
- Plasmid 2
- Total: about 7443bp
- In order to create plasmid 2 (4 patterns), GFAPpromoter, HlyD, HlyB, TolC, and HlyA + IL-12 or GFP were cloned.
- This four plasmids has the same molecular weight.
- The four figure below shows colony observation image obtained by binding all genes and inserts them in pSB1C3 and transforms them into DH5α.
- Agarose gel electrophoresis result of plasmid extraction from the obtained colonies is shown in figure below.
- From figure above, we can confirm that all the plasmids obtained are plasmid 2 since the molecular weight is consistent with the molecular weight targeted.
Contact: kaitjapan@gmail.com Twitter:@KAIT_JAPAN