In all ligand titrations, the concentration of ligand isvaried around the KD of the complex. In a stoichiometric titration,what is the concentration of receptor in relationship to KD? Howdoes this differ from a binding titration experiment? Can you get aKD from a stoichiometric binding Titration? Why do thestoichiometric titration experiment this way, and what kind ofinformation does it give you?
