Difference between revisions of "Team:San Andres/Modeling"

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      <a href="https://2015.igem.org/Team:San_Andres/Description"
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          <a href="https://2015.igem.org/Team:San_Andres" style="color: rgb(0, 0, 0);">Home </a>  
style="color: rgb(0, 0, 0);"> Project </a>
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          <a href="https://2015.igem.org/Team:San_Andres/Description" style="color: rgb(0, 0, 0);"> Project </a>
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style="color: rgb(0, 0, 0);"> Statistics</a>
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          <a href="https://2015.igem.org/Team:San_Andres/Notebook" style="color: rgb(0, 0, 0);"> Statistics</a>
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style="color: rgb(0, 0, 0);"> Enzymes</a>
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          <a href="https://2015.igem.org/Team:San_Andres/Parts" style="color: rgb(0, 0, 0);"> Parts</a>
      </td>
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        </td>
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          <a href="https://2015.igem.org/Team:San_Andres/Modeling" style="color: rgb(0, 0, 0);"> Metodology</a>
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      <a href="https://2015.igem.org/Team:San_Andres/Parts"
+
          <a href="https://2015.igem.org/Team:San_Andres/Results" style="color: rgb(0, 0, 0);"> Results </a>
style="color: rgb(0, 0, 0);"> Parts</a>
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      </td>
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      <td style="border: 2px solid black;"
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          <a href="https://2015.igem.org/Team:San_Andres/Collaborations" style="color: rgb(0, 0, 0);"> Future Projections </a>
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          <a href="https://igem.org/Team_List?year=2015">
      <a href="https://2015.igem.org/Team:San_Andres/Notebook"
+
            <img src="https://static.igem.org/mediawiki/igem.org/6/60/Igemlogo_300px.png" width="55">
style="color: rgb(0, 0, 0);"> Metodology</a>
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      <a href="https://2015.igem.org/Team:San_Andres/Results"
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      <a href="https://2015.igem.org/Team:San_Andres/Collaborations"
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style="color: rgb(0, 0, 0);"> Future Projections </a>
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      <td align="center">
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      <a href="https://igem.org/Team_List?year=2015"><img
+
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Revision as of 14:39, 14 July 2015

wiki wiki 2

Home Team Project Statistics Enzymes Parts Metodology Results Future Projections

Metodology 

The methodology consists of cutting and pasting, with ligases and restriction enzymes as a "waterfall", for final assembly that will produce both proteins. The motive of this assembly is due to the fact that the promoter, the RBS and the terminator were too small, and if you take out them from their original plasmids, these are lost, so, simply sticking and peeling it off one by one, we arrived to a linear Assembly in the three corresponding plasmids (promoter, RBS and terminator).

File:Modelo cascada.jpg
At this time we are innovating ideas to add a circuit that will allow us in the future to obtain a method of detecting and quantifying the presence of gluten, which can also be checked by a commercial kit.

File:Kit gluten.jpg