Team:NYMU-Taipei/modeling/m7

From 2014.igem.org

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<p>The circuit is constructed by the following parts, constitutive promoter + rbs + INPNC (k523013) + C16 + terminator (B0015). The detailed mechanism is introduced on <a href='/Team:NYMU-Taipei/project/2c1'><b>Cleanse-Attachment</b></a>.</p>
<p>The circuit is constructed by the following parts, constitutive promoter + rbs + INPNC (k523013) + C16 + terminator (B0015). The detailed mechanism is introduced on <a href='/Team:NYMU-Taipei/project/2c1'><b>Cleanse-Attachment</b></a>.</p>
</p>
</p>
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<p>In this part, we fit the parameter in the system with the experimental data from our wet lab. The amount of protein expression is transferred from the florescence [1]. </p>
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<p>In this part, we fit the parameter in the system with the experimental data from our wet lab. To test how the circuit works, GFP is added after C16 in the testing circuit. It can represent the amount of C16 protein. The amount of protein expression is transferred from the GFP florescence [1].</p>
       <h1>System</h1>
       <h1>System</h1>
       <h1>Result</h1>
       <h1>Result</h1>

Revision as of 13:34, 10 October 2014

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New part:Attachment

Introduction

This part aims to simulate the circuit of Attachment part, which can help shorten the distance of helper E. coli and S. mutans.

The circuit is constructed by the following parts, constitutive promoter + rbs + INPNC (k523013) + C16 + terminator (B0015). The detailed mechanism is introduced on Cleanse-Attachment.

In this part, we fit the parameter in the system with the experimental data from our wet lab. To test how the circuit works, GFP is added after C16 in the testing circuit. It can represent the amount of C16 protein. The amount of protein expression is transferred from the GFP florescence [1].

System

Result

Reference

  1. H. A. Richards, Quantitative GFP fluorescence as an indicator of recombinant protein synthesis in transgenic plants. Plant Cell Rep (2003) 22:117–121

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