1978
DOI: 10.1042/bj1750029
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Isolation and characterization of the subunits of bovine follitropin

Abstract: Highly purified bovine follitropin was dissociated into its alpha- and beta-subunits after treatment with 1 M-propionic acid. The dissociated subunits were fractionated by chromatography on DEAE-cellulose and further purified by gel filtration on Sephadex G-100. The isolated alpha- and beta-subunits were biologically inactive, but their recombinants regenerated 80% of the follitropin activity. The alpha-subunit of bovine follitropin recombined with the beta-subunits of bovine lutropin and thyrotropin to regene… Show more

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Cited by 5 publications
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“…1). The specificity of this antiserum for bovine FSH has been fully characterized (Cheng, 1978a), and the chemical nature of bovine and ovine FSH has been shown to be very similar (Cheng, 1976(Cheng, , 1978b (Cheng, 1976). It has generally been established that immunoassays and receptor assays measure different aspects of the configuration of the protein and this may account for the differences of measurements by these systems.…”
Section: Discussionmentioning
confidence: 99%
“…1). The specificity of this antiserum for bovine FSH has been fully characterized (Cheng, 1978a), and the chemical nature of bovine and ovine FSH has been shown to be very similar (Cheng, 1976(Cheng, , 1978b (Cheng, 1976). It has generally been established that immunoassays and receptor assays measure different aspects of the configuration of the protein and this may account for the differences of measurements by these systems.…”
Section: Discussionmentioning
confidence: 99%