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<h1>Results&nbsp;</h1>
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<div style="text-align: justify; font-family: Cambria;"><big>We
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have our final plasmid. In the graphic model we can visualize the
 
have our final plasmid. In the graphic model we can visualize the
 
promoter, the RBS, the enzyme KumaMax, the RFP and the terminator</big>.
 
promoter, the RBS, the enzyme KumaMax, the RFP and the terminator</big>.
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<div style="text-align: justify;"><big>These results
 
<div style="text-align: justify;"><big>These results
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ideas to add a circuit that will allow us in the future to get a method
 
ideas to add a circuit that will allow us in the future to get a method
 
to detect and quantify the presence of gluten, which can also be
 
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Revision as of 01:53, 15 September 2015

<endnote><head> <title><endnote><head> <meta> <title> wiki wiki exp wiki wiki wiki 2   File:Gluten-s-Job.jpeg

Home Team Project Parts Modeling Results
Notebook Human Practices Future Projections Attributions Collaborations

Results 

We currently have our final plasmid. In the graphic model we can visualize the promoter, the RBS, the enzyme KumaMax, the RFP and the terminator.

File:Circulo.png

These results are expected to occupy it in a drug for celiac disease. The plasmid that  we have built indicates that it is degrading gluten, but not if it is degraded completely. For this reason we are innovating ideas to add a circuit that will allow us in the future to get a method to detect and quantify the presence of gluten, which can also be checked via a commercial kit.
https://static.igem.org/mediawiki/2015/thumb/5/58/Cage1.png/800px-Cage1.png