Difference between revisions of "Team:Gifu/team-profile"
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splicing were far each other. So we incorporated complementary sequences around the ribozyme regions. We thought that | splicing were far each other. So we incorporated complementary sequences around the ribozyme regions. We thought that | ||
the treatment brought two regions close and the efficiency of the circularization improved.<br> | the treatment brought two regions close and the efficiency of the circularization improved.<br> | ||
− | The other was to synthesize useful proteins. In our previous study, synthesized long-chain proteins lose their function | + |  The other was to synthesize useful proteins. In our previous study, synthesized long-chain proteins lose their function |
because the folding of the proteins was broken. So we incorporated linker sequences into circular mRNA to synthesize the | because the folding of the proteins was broken. So we incorporated linker sequences into circular mRNA to synthesize the | ||
functional long-chain protein.<br></tr></tbody></table><br> | functional long-chain protein.<br></tr></tbody></table><br> |
Revision as of 01:24, 18 September 2015
TEAM PROFILE
Team Name: | Gifu | ||||||||
Primary Contact (PI): | Hitoshi IWAHASHI | ||||||||
Schools: | Gifu University Yanagido, Gifu, Japan | ||||||||
Division: | iGEM | Application Date: 2015-04-27 | |||||||
Section: | Undergraduate | ||||||||
Region: | Asia | Acceptance Date: 2015-05-02 08:32:07 | |||||||
Description: |
Team Status |
Welcome to iGEM 2015 ! Your iGEM 2015 team application was accepted by iGEM Headquarters on 2015-05-02 08:32:07 and your team registration fee has been received. |
DNA Kit of Parts shipping information has been entered, thanks. View shipping information |
Resource description has been submitted, thanks. View resource description |
Your registration fee has been received. Thank you.
More... |
TrackMore... |
Assigned Track: New Application |
Title and AbstractMore... | Download a .pdf version |
Circular mRNA ver2 | ||||||||
In last year, we succeeded in designing the sequence which synthesizes circular mRNA and long chain protein in
Escherichia coli. In this year, we had 2 purposes in our study. One was an efficiency of the circularization. The efficiency was lower in our previous study. This was why the splicing was hard to happen because two sequences to act as ribozyme for splicing were far each other. So we incorporated complementary sequences around the ribozyme regions. We thought that the treatment brought two regions close and the efficiency of the circularization improved. The other was to synthesize useful proteins. In our previous study, synthesized long-chain proteins lose their function because the folding of the proteins was broken. So we incorporated linker sequences into circular mRNA to synthesize the functional long-chain protein. |
Team Roster |
Instructors | |||
aebihara2015 | Akio Ebihara | ||
isatoshi | Satoshi IWAMOTO | ||
h1884 | Hitoshi IWAHASHI |
Student Members | |||
ybanno | Yusuke Banno | ||
nomuken | Nomura Kenta | ||
momochi | Momoko YAMADA | ||
kozakai | Kozakai Tomoya | ||
Mori | Akihiro Moriyama | ||
Yuki1201 | Yuki Kamijo | ||
SachiA | Sachi Asano | ||
takema | Hasegawa Takema | ||
fukufuku | Wataru Fukuda | ||
Lagomutry | Ouchi Ryo | ||
uyuu | Endo Yuki |
This range of part numbers has been assigned to your team for use during the summer: BBa_K1332000 to BBa_K1332999 |