Difference between revisions of "Team:ETH Zurich/Lab"

Line 30: Line 30:
 
<div class="imgBox" style="width:90%;margin: 20px auto 20px auto !important;">
 
<div class="imgBox" style="width:90%;margin: 20px auto 20px auto !important;">
 
<a href="https://static.igem.org/mediawiki/2015/6/6a/ETH15_coculture_overview.png">
 
<a href="https://static.igem.org/mediawiki/2015/6/6a/ETH15_coculture_overview.png">
<img src="hhttps://static.igem.org/mediawiki/2015/6/6a/ETH15_coculture_overview.png">
+
<img src="https://static.igem.org/mediawiki/2015/6/6a/ETH15_coculture_overview.png">
 
</a>
 
</a>
<p><b><a href="https://2015.igem.org/Team:ETH_Zurich/Results#Mammalian_cells_and_bacteria_combined">Coculture</a> of bacteria and mammalian cells.</b></p>
+
<p><a href="https://2015.igem.org/Team:ETH_Zurich/Results">Coculture</a> of mammalian cells with <i>E. coli</i>. </p>
 
</div>
 
</div>
  

Revision as of 21:31, 17 September 2015

"What I cannot create I do not understand."
- Richard Feynmann

Lab

Overview

In the wet lab we worked with mammalian cell culture, did a lot of experiments and cloning with E. coli, developped and tested a microfluidics chip and, last but not least, we combined all these three parts to test our system. We invested a lot of time and effort into the generation of reliable data sets and never stopped looking for more experiments that would make it possible for us to achieve the most fruitful interaction with the modeling team, which in turn helped us a lot in setting a focus on critical points.

Coculture of mammalian cells with E. coli.

Please take a look at our experimental Results to see how we achieved

Moreover, we are desinged a testing system of our final test setup in a Microfluidic Chip. More informations about the performed experimetns can be found on our Experiments page. In addition, an overview over the bacterial strains and mammalian cell lines we used for our experiments, along with a list of materials and equipment can be found in our Materials page.

We are one of 71 teams that participated at this years Interlab Study, in which we measrued the fluorescence ot the three test constructs using FACSflow cytometry, as well as our microtiter plate reader.

We would like to thank our sponsors