Difference between revisions of "Team:KU Leuven/Wetlab"

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  <h2>Plasmids</h2>
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<p>“ We are not gonna buy that; We can make it “
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When designing plasmids, we need to add tags and fluorescent proteins to quantify our parameters. We will also add extra restriction sites to easily generate biobricks.
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<a href="https://2015.igem.org/Team:KU_Leuven/Wetlab/About">Read more</a>
 
<a href="https://2015.igem.org/Team:KU_Leuven/Wetlab/About">Read more</a>
 
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  <h2>Experiments</h2>
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  <h2>Parts</h2>
  <p>Here you can find the following steps to become our modified organism and detailed quantification methods to determine interesting parameters.
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<a href="https://2015.igem.org/Team:KU_Leuven/Project/About">Read more</a>
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<h2>Methods</h2>
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  <p>The used methods.  
 
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<a href="https://2015.igem.org/Team:KU_Leuven/Project/About">Read more</a>
 
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  <h2>Results</h2>
 
  <h2>Results</h2>
  <p>The results of our experiments will appear here.
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  <p>The results obtained in our project
 
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<a href="https://2015.igem.org/Team:KU_Leuven/Project/About">Read more</a>
 
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Revision as of 13:09, 28 July 2015

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Research

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We designed a circuit capable of producing patterns in a controlled way. Using a modified and temperature-sensitive lambda repressor (cI), we can trigger this structure formation at desired points in time. This time-dependent controllability, together with the possibility to change many different parameters and output signals, leads to an enormous tunability in the creation of the patterns, providing advancements in a variety of industrial processes like for example the creation of novel bio-materials. On the other hand, this fundamental project could also speed up medical research projects on among others tumor formation and tissue regeneration.

Background

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Parts

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Methods

The used methods.
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Results

The results obtained in our project
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