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- W2046065012 abstract "Sex hormone-binding globulin (SHBG) is conventionally measured by saturation of binding sites with 5cu-dihydrotestosterone (DHT) of known specific activity followed by separation of the bound and free steroid fractions. The techniques used for separation cf these fractions vary and the reference ranges obtained for normal subjects are not in agreement (1, 2 and refs. cited therein]. More recently, antibodies raised against purified SHBG have been used in radioimmunologic and immunodiffusion assays [2-71. Although some antisera contained immunoglobulin G and transferrin antibodies [5,8-lo], several workers have produced monospecific antisera [3,5,7]. A partially characterized murine monoclonal antibody has been reported [ll]. These antibody-based assays are not without problems. Highly purified SHBG may progressively lose binding capacity [3] and immunological activity [2] and can be extensively damaged by radioiodination [4]. Recently, a commercial kit using a radiolabelled monoclonal antibody to SHBG which recognizes a discrete determinant on the molecule has been produced. We have compared this kit with the commonly used binding assay, using ammonium sulfate to separate bound from free steroid." @default.
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- W2046065012 title "Comparison of DHT-binding and monoclonal immunoradiometric methods for the measurement of sex hormone-binding globulin" @default.
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- W2046065012 doi "https://doi.org/10.1016/0009-8981(85)90058-0" @default.
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