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Monohydrogen phosphate
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Equilibrium Dissociation constant, pKa H3PO4 ⇌ H 2PO− 4 + H+ pKa1 = 2.14 H 2PO− 4 ⇌ HPO2− 4 + H+ pKa2 = 7.20 HPO2− 4 ⇌ PO3− 4 + H+ pKa3 = 12.37Kinetic exclusion assay (2,009 words) [view diff] exact match in snippet view article find links to article
series of equilibrated solutions enables calculation of the equilibrium dissociation constant (Kd). Measuring the free receptor with several points beforeSurface plasmon resonance (3,654 words) [view diff] exact match in snippet view article find links to article
the affinity between two ligands involves establishing the equilibrium dissociation constant, representing the equilibrium value for the product quotientPharmacodynamics (2,580 words) [view diff] exact match in snippet view article find links to article
determine the equilibrium concentration of bound receptors. The equilibrium dissociation constant is defined by: L + R ↽ − − ⇀ LR {\displaystyle {\ce {L + RProtein–ligand complex (1,297 words) [view diff] exact match in snippet view article find links to article
The affinity between protein and ligand is given by the equilibrium dissociation constant Kd or the inverse of the association constant 1/Ka (or bindingReceptor theory (2,007 words) [view diff] exact match in snippet view article find links to article
receptor, but also the active receptor (R*). The model uses an equilibrium dissociation constant to describe the interaction between ligand and receptor. ItPhosphate (2,540 words) [view diff] case mismatch in snippet view article find links to article
Equilibrium Dissociation constant Ka pKa H3PO4 ⇌ H2PO−4 + H+ K a 1 = [ H + ] [ H 2 PO 4 − ] [ H 3 PO 4 ] ≈ 7.5 × 10 − 3 {\displaystyle K_{a1}={\frac {[{\ceLogan plot (1,373 words) [view diff] exact match in snippet view article find links to article
of ligand binding sites, K d {\displaystyle K_{d}} is the equilibrium dissociation constant for the ligand-binding site complex, k o n {\displaystyleAsKC11 (1,177 words) [view diff] exact match in snippet view article find links to article
rate constant (Koff = β) is 6.33 x 10−3 s−1. The calculated equilibrium dissociation constant to represent the affinity of AsKC11 to GIRK1/2 channels hasChemical specificity (2,057 words) [view diff] exact match in snippet view article find links to article
but not cellulose (because it is a beta-linkage). Specific equilibrium dissociation constant for formation of the enzyme-substrate complex is known asSBP-tag (1,719 words) [view diff] exact match in snippet view article find links to article
The SBP-Tag has been shown to bind streptavidin with an equilibrium dissociation constant of 2.5nM and is readily eluted with biotin under native conditionsCarbon monoxide-releasing molecules (2,378 words) [view diff] exact match in snippet view article find links to article
approximately 210x greater affinity for hemoglobin than oxygen. The equilibrium dissociation constant for the reaction Hb-CO ⇌ Hb + CO strongly favours the CO complexPhenylalanine (2,387 words) [view diff] exact match in snippet view article find links to article
binding site of NMDA receptor L-phenylalanine has an apparent equilibrium dissociation constant (KB) of 573 μM estimated by Schild regression which is considerablyNMDA receptor antagonist (4,196 words) [view diff] exact match in snippet view article find links to article
(ACPC). L-Phenylalanine. a naturally occurring amino acid (equilibrium dissociation constant (KB) from Schild regression is 573 μM). Xenon: an anestheticRadioligand (4,347 words) [view diff] exact match in snippet view article find links to article
Depiction of a Scatchard plot with relation to number of binding sites, Bmax, and equilibrium dissociation constant Kd.Nucleoid (17,312 words) [view diff] exact match in snippet view article find links to article
the E. coli cell to be 2 μm3. 1 Binding affinity refers to equilibrium dissociation constant (Kd) in molar units (M). ND = not determined Histone-likePharmacodynamics of estradiol (12,043 words) [view diff] exact match in snippet view article find links to article
characteristically exhibit high affinity for estradiol-17J3, with an equilibrium dissociation constant of 0.1 nM. The number of these sites in target tissues is