Team:ULB-Brussels/Modelling

From 2014.igem.org

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<h1>S</h1>
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<h3>Population Dynamics Model</h3>
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<p>The growth of bacteria.</p>
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<h3>Toxin-Antitoxin Systems</h3>
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<p>Two type II TA systems have been planned to be investigated in our project.</p>
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The first consist of ccdB (the toxin, T) and ccdA (the antitoxin, A) and for the second, these are Kid (T) and Kis (A).</p>
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Revision as of 07:25, 9 August 2014

$~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\MyColi}{{\small Mighty\hspace{0.12cm}Coli}} \newcommand{\Stabi}{\small Stabi}$ $\newcommand{\EColi}{\small E.coli} \newcommand{\SCere}{\small S.cerevisae}\\[0cm] ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ \newcommand{\PI}{\small PI}$ $\newcommand{\Igo}{\Large\mathcal{I}} \newcommand{\Tgo}{\Large\mathcal{T}} \newcommand{\Ogo}{\Large\mathcal{O}} ~$ Example of a hierarchical menu in CSS

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- Université Libre de Bruxelles -



Modelling


S

Population Dynamics Model

The growth of bacteria.

Toxin-Antitoxin Systems

Two type II TA systems have been planned to be investigated in our project.

The first consist of ccdB (the toxin, T) and ccdA (the antitoxin, A) and for the second, these are Kid (T) and Kis (A).

In this page, the modelling part will be detailed with previews about our biological system and the results with numerical simulations of bacteria populations and structural components of the chosen plasmids.

Afterwards, these simulations will be compared with experimental results. In parallel, an estimation of the production in sub-populations cells in bioreactors by coupling the recombinant protein with an essential protein and a numerical estimation will be purposed. Now, we're beginning to perform it.




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