Difference between revisions of "Team:Stuttgart/Collaborations"
Heidi Muehl (Talk | contribs) |
|||
| Line 725: | Line 725: | ||
<br> | <br> | ||
<br><h1 align=middle>Collaborations with other iGEM-Teams</h1> | <br><h1 align=middle>Collaborations with other iGEM-Teams</h1> | ||
| − | + | ||
<table> | <table> | ||
| − | |||
| − | |||
| + | <td align="left" bgcolor="#F8CE63" width=30% height=30%> | ||
| + | <br> | ||
| + | Being the first team at the University of Stuttgart we were confrontated with a lot of starting problems. But we were welcomed so friendly! Everone gave us good advice, shared their experiences with sponsors, iGEM itself or solving experimental problems. We met a few german teams to exchange information and to just have a good time with each other. All in all it was a very valuable experience to us. <br> | ||
| + | So – big thanks to all iGEM-Teams for the support and helpful hints. It made the start much more easier and we are happy to be part of that great iGEM-community now. | ||
| + | <br> | ||
</td> | </td> | ||
<td align=left width=30% height=30% bgcolor=#190707> | <td align=left width=30% height=30% bgcolor=#190707> | ||
| + | <h4><span style="color:#F8CE63">The project of this year’s iGEM-team in Heidelberg is about accelerated evolution using phage-assisted continuous evolution (PACE). This is a very fast method to insert a desired mutation into bacterial cells. In their case, they used the method to evolve three mutagenesis plasmids developing different antibiotic resistances in E. coli cells. We were asked to perform a mutagenesis plasmid activity assay to analyze their function and mutagenesis levels. In return they supported us developing our safety part. Based on their suggestions we designed our light-induced killswitch. <br> | ||
| + | All in all Team Heidelberg gave us continuous support and we are very thankful for that.</span style="color:#F8CE63"> <br><br> | ||
| + | <span style="color:#F8CE63">for more information check out their wiki <a href="https://2017.igem.org/Team:Heidelberg">page</a></span style="color:#F8CE63"></h4> | ||
| + | <br> | ||
<h4><span style="color:#F8CE63"><li>iGEM-Team Cologne-Duesseldorf --> check out their wiki <a href="https://2017.igem.org/Team:Cologne-Duesseldorf">page</a></li></span style="color:#F8CE63"></h4> | <h4><span style="color:#F8CE63"><li>iGEM-Team Cologne-Duesseldorf --> check out their wiki <a href="https://2017.igem.org/Team:Cologne-Duesseldorf">page</a></li></span style="color:#F8CE63"></h4> | ||
<br> | <br> | ||
<h4><span style="color:#F8CE63"><li>iGEM-Team Canmore 2016 --> check out their wiki <a href="https://2016.igem.org/Team:OLS_Canmore">page</a></li></span style="color:#F8CE63"></h4> | <h4><span style="color:#F8CE63"><li>iGEM-Team Canmore 2016 --> check out their wiki <a href="https://2016.igem.org/Team:OLS_Canmore">page</a></li></span style="color:#F8CE63"></h4> | ||
| − | |||
| − | |||
<br> | <br> | ||
<h4><span style="color:#F8CE63"><li>iGEM-Team Tübingen--> check out their wiki <a href="https://2017.igem.org/Team:Tuebingen">page</a></li> | <h4><span style="color:#F8CE63"><li>iGEM-Team Tübingen--> check out their wiki <a href="https://2017.igem.org/Team:Tuebingen">page</a></li> | ||
</td></span style="color:#F8CE63"></h4> | </td></span style="color:#F8CE63"></h4> | ||
<br> | <br> | ||
| − | + | ||
</table> | </table> | ||
Revision as of 16:01, 29 October 2017
Collaborations with other iGEM-Teams
|
Being the first team at the University of Stuttgart we were confrontated with a lot of starting problems. But we were welcomed so friendly! Everone gave us good advice, shared their experiences with sponsors, iGEM itself or solving experimental problems. We met a few german teams to exchange information and to just have a good time with each other. All in all it was a very valuable experience to us. So – big thanks to all iGEM-Teams for the support and helpful hints. It made the start much more easier and we are happy to be part of that great iGEM-community now. |
The project of this year’s iGEM-team in Heidelberg is about accelerated evolution using phage-assisted continuous evolution (PACE). This is a very fast method to insert a desired mutation into bacterial cells. In their case, they used the method to evolve three mutagenesis plasmids developing different antibiotic resistances in E. coli cells. We were asked to perform a mutagenesis plasmid activity assay to analyze their function and mutagenesis levels. In return they supported us developing our safety part. Based on their suggestions we designed our light-induced killswitch.
|
