Team:ULB-Brussels/Modelling

From 2014.igem.org

(Difference between revisions)
Line 11: Line 11:
<table style="background-color:#ebebeb;" width="90%"  align="center">
<table style="background-color:#ebebeb;" width="90%"  align="center">
<tr style="background-color:rgb(245,245,245);"><td>
<tr style="background-color:rgb(245,245,245);"><td>
-
<section style="text-align: justify; margin: 25px"><p>In this page, the modelling part will be detailed with previews about our biological system and the results with numerical simulations of populations of bacteria and structural components of the chosen plasmids.</p>
+
<section style="text-align: justify; margin: 50px"><p>In this page, the modelling part will be detailed with previews about our biological system and the results with numerical simulations of populations of bacteria and structural components of the chosen plasmids.</p>
<p>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.</p>
<p>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.</p>

Revision as of 16:31, 4 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

carousel slider




- Université Libre de Bruxelles -



Modelling


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