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Hi,
Im new here! Having some problems with a radioligand binding assay, namely im wondering whether or not to use a competitive scheme to determine the Kd for a compound from my enzyme. I have relatively little radiolabeled ligand, so I have to use it rather conservatively. So why not use a constant concentration and then add specific amounts of unlabeled ligand? Im not sure if this is acceptable though...Anyone have any suggestions? thanks. |
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