Team:Paris/Modeling/f2
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No particular strain. | No particular strain. | ||
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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] = ƒ2(TetR) = ƒ2aux(IPTG), we can study [expr.''Ptet''] = ƒ2ter([TetR],[aTc]), and determine by calcul [TetR<sub>active</sub>] = ƒ2bis(aTc) = f2<sup>-1</sup>([expr.''Ptet'']), to endly give an analytical expression of ƒ2ter = ƒ2οƒ2bis | 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 [TetR<sub>active</sub>] = ƒ2bis(aTc) = f2<sup>-1</sup>([expr.''Ptet'']), to endly give an analytical expression of ƒ2ter = ƒ2οƒ2bis |
Revision as of 16:24, 12 August 2008
No particular strain.
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] = 2(TetR) = 2aux(IPTG), we can study [expr.Ptet] = 2ter([TetR],[aTc]), and determine by calcul [TetRactive] = 2bis(aTc) = f2-1([expr.Ptet]), to endly give an analytical expression of 2ter = 2ο2bis