“…Despite the low affinity of LR 3 IGF-I for IGF-binding proteins, these binding proteins interfere in the LR 3 IGF-I RIA in much the same way as they do in RIAs for IGFs-I and -II unless they are removed prior to assay (Daughaday et al 1987, Breier et al 1991. The preferred method for achieving this is chromatographic extraction under acidic, dissociating conditions before RIA (Hintz & Liu 1977, Powell et al 1986, Daughaday et al 1987, Breier et al 1991, Crawford et al 1992). Here we describe the development, performance and characteristics of a nonisotopic assay of LR 3 IGF-I in blood plasma that does not require sample extraction.…”