Team:Paris/Modeling/f2

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[[Image:f2.png]]
[[Image:f2.png]]
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Exactly as for the binding of IPTG on LacR, leading to a lowered inhibition of p-lac, aTc binds to TetR. So, after having determinated the Hill function [expr.p-tet] = f2(TetR) = f2bis(IPTG), we can study [expr.p-Tet] = f2(TetR,aTc), and determine by calcul TetR_{active} = f2ter(aTc) = f2^{-1}([expr.p-tet]).
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Exactly as for the binding of IPTG on LacR, leading to a lowered inhibition of p-lac, aTc binds to TetR. So, after having determinated the Hill function [expr.p-tet] = &#131;2(TetR) = &#131;2aux(IPTG), we can study [expr.''Ptet''] = &#131;2ter([TetR],[aTc]), and determine by calcul [TetR<sub>active<sub>] = &#131;2bis(aTc) = f2<sup>-1</sup>([expr.''Ptet'']), to endly give an analytical expression of &#131;2ter = &#131;2&#186;&#131;2bis

Revision as of 15:50, 1 August 2008

No particular strain.

F2.png

Exactly as for the binding of IPTG on LacR, leading to a lowered inhibition of p-lac, aTc binds to TetR. So, after having determinated the Hill function [expr.p-tet] = ƒ2(TetR) = ƒ2aux(IPTG), we can study [expr.Ptet] = ƒ2ter([TetR],[aTc]), and determine by calcul [TetRactive] = ƒ2bis(aTc) = f2-1([expr.Ptet]), to endly give an analytical expression of ƒ2ter = ƒ2ºƒ2bis

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