Team:NYMU-Taipei/modeling/m7

From 2014.igem.org

(Difference between revisions)
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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>
<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>
 +
      <p>INPNC, C16, and GFP are the main product in the testing circuit. In the design circuit, there are only INPNC and C16. GFP can be used to test whether the circuit is functional.
 +
$$\frac{d[\text{GFP mRNA}]}{dt}=P_{const}-K_{deg_mGFP}[\text{GFP mRNA}]$$
 +
$$\frac{d[\text{GFP}]}{dt}=K_t[\text{GFP mRNA}]-K_{deg_GFP}[GFP]$$
 +
</p>
       <h1>Result</h1>
       <h1>Result</h1>
       <h1>Reference</h1>
       <h1>Reference</h1>

Revision as of 13:47, 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

INPNC, C16, and GFP are the main product in the testing circuit. In the design circuit, there are only INPNC and C16. GFP can be used to test whether the circuit is functional. $$\frac{d[\text{GFP mRNA}]}{dt}=P_{const}-K_{deg_mGFP}[\text{GFP mRNA}]$$ $$\frac{d[\text{GFP}]}{dt}=K_t[\text{GFP mRNA}]-K_{deg_GFP}[GFP]$$

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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