Author:
Wilkinson M L,Iqbal M J,Forbes A,Corbishley T P,Williams R
Abstract
In order to develop an immunoassay for foetal steroid-binding protein in human serum, which is impossible to assay quantitatively in normal samples by conventional ligand-binding techniques, the protein was purified by salt precipitation, affinity chromatography and gel filtration. Elution was by competing ligand or alkaline pH. The purified protein was further characterized and a highly specific antiserum was raised in rabbits.
Subject
Cell Biology,Molecular Biology,Biochemistry
Cited by
4 articles.
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