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

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<h2>Overview</h2>
 
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<p>In the wet lab we worked with <b>mammalian cell culture</b>, did a lot of experiments and cloning with <b><i>E. coli</i></b>, developped and tested a <b>microfluidics chip</b> and, last but not least, we <b>combined all these three parts</b> 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 <a href="https://2015.igem.org/Team:ETH_Zurich/Modeling">modeling</a> team, which in turn helped us a lot in setting a focus on critical points.</p>
<p>The wet lab work we did in the course of this project was as <b>diverse</b> as it can possibly be. We worked with <b>mammalian cell culture</b>, did a lot of experiments and cloning with <b><i>E. coli</i></b>, developped and tested a <b>microfluidics chip</b> and, last but not least, we <b>combined all these three parts</b> to test our system. We invested a lot of time into the generation of reliable data sets and never stopped looking for more experiments to do that would make it possible for us to achieve the most fruitful interaction with the <a href="https://2015.igem.org/Team:ETH_Zurich/Modeling">modeling</a> team, which in turn helped us a lot in setting a focus on critical points.</p>
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<li>the characterization of 15 newly designed <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Characterization_of_the_LldR_promoter">promoters controlled by LldR and Lactate</a></li>
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<li>the characterization of 15 newly designed <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Characterization_of_the_LldR_promoter">promoters controlled by the regulator LldR and it's inhibitor L-lactate</a></li>
 
<li>the characterization of 2 newly designed <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Characterization_of_the_lacI-lldR_promoter">hybrid promoters</a>, combining repression by LldR and LacI</li>
 
<li>the characterization of 2 newly designed <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Characterization_of_the_lacI-lldR_promoter">hybrid promoters</a>, combining repression by LldR and LacI</li>
 
<li>the closer elucidation of the <b>poorly characterized</b> mechanism of action behind the <a href="https://2015.igem.org/Team:ETH_Zurich/Modeling/Lactate_Module#A_closer-look_at_the_mechanism_of_LldR">LldR-mediated repression</a> of the LldR-operator-promoter</li>
 
<li>the closer elucidation of the <b>poorly characterized</b> mechanism of action behind the <a href="https://2015.igem.org/Team:ETH_Zurich/Modeling/Lactate_Module#A_closer-look_at_the_mechanism_of_LldR">LldR-mediated repression</a> of the LldR-operator-promoter</li>
 
<li>the investigation of <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Mammalian_cells_and_bacteria_combined">binding of bacteria to apoptotic mammalian cells</a></li>
 
<li>the investigation of <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Mammalian_cells_and_bacteria_combined">binding of bacteria to apoptotic mammalian cells</a></li>
<li>the validation of a tight <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Quorum_sensing_modul">AND gate</a></li>
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<li>the validation of a tight <a href="https://2015.igem.org/Team:ETH_Zurich/Results#Quorum_sensing_modul">AND gate</a> with a clear binary behaviour</li>
 
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Revision as of 23:26, 16 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.

placeholder. put nice cells and make it bigger

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