|
|
Line 196: |
Line 196: |
| | | |
| <!-- Non-editable Member 24761 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=21240">FreshLemon</a><td style="width: 200px;">Haruka Maruyama<td><td> | | <!-- Non-editable Member 24761 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=21240">FreshLemon</a><td style="width: 200px;">Haruka Maruyama<td><td> |
− | </tr></tbody></table><br>
| |
| | | |
| <!-- Non-editable Member 23901 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=20597">takema</a><td style="width: 200px;">Hasegawa Takema<td><td> | | <!-- Non-editable Member 23901 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=20597">takema</a><td style="width: 200px;">Hasegawa Takema<td><td> |
Line 208: |
Line 207: |
| <!-- Non-editable Member 23900 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=20595">SachiA</a><td style="width: 200px;">Sachi Asano<td><td> | | <!-- Non-editable Member 23900 --><tr><td style="width: 150px; padding-left: 10px;"><a href="User_Information.cgi?user_id=20595">SachiA</a><td style="width: 200px;">Sachi Asano<td><td> |
| | | |
| + | </tr></tbody></table><br> |
| | | |
| | | |
Revision as of 01:45, 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: |
|
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. |
Assigned Track: New Application
|
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.
|
| FreshLemon | Haruka Maruyama | |
|
takema | Hasegawa Takema | |
|
ybanno | Yusuke Banno | |
|
Mori | Akihiro Moriyama | |
|
fukufuku | Wataru Fukuda | |
|
SachiA | Sachi Asano | |
|
This range of part numbers has been assigned to your team for use during the summer: BBa_K1332000 to BBa_K1332999
|