Team:Paris/Modeling/f2

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(New page: No particular strain. Image: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 fun...)
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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 apply the same method as for the [expr.p-lac] = f1bis(LacR) = f1(IPTG), in order to find [expr.p-lac] = f2(TetR,aTc).
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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]).

Revision as of 15:36, 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] = 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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