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Estriol in pregnancy. III. Development, comparison and use of specific antisera for rapid radioimmunoassay of unconjugated estriol in pregnancy plasma
Authors:H Katagiri  F Z Stanczyk  U Goebelsmann
Institution:Department of Obstetrics and Gynecology University of Southern California School of Medicine and Los Angeles County-USC Medical Center U.S.A.
Abstract:Estriol-6-(0-carboxymethyl) oxime (E3-CMO) and estriol-4-azobenzoic acid (E3-4-ABA) were linked to bovine serum albumin (BSA). Twelve rabbits were immunized, six with each E3-BSA conjugate. All six E3-6-CMO-BSA rabbits, but only one E3-4-ABA-BSA animal, responded with useful antibody titers. All antisera exhibited good Ring D specificity. E3-6-CMO-BSA (type 1) antisera cross-reacted up to 220 percent with 6-oxoestriol while the E3-4-ABA-BSA (type 2) antiserum cross-reacted only 3.8 percent with this steroid. Neither type of antiserum cross-reacted with neutral steroids nor with estriol-16-glucosiduronate and estriol-3-sulfate-16-glucosiduronate, but both cross-reacted with estriol-3-sulfate and estriol-3-glucosiduronate.Both types of antisera could be utilized for a rapid and specific radioimmunoassay (RIA) of unconjugated E3 in third trimester pregnancy plasma without need for further purification of the plasma extract. Blanks were negligible, sensitivity was sufficient, recovery was virtually complete by using 3H-E3 as an internal standard, and precision was satisfactory. The measurements of unconjugated plasma E3 concentrations in ninety apparently normal women between 29 and 40 weeks or gestation obtained by this RIA averaged 7.6, 10.2 and 16.7 ng/ml at 29 to 32, 33 to 36 and 37 to 40 weeks of gestation, respectively.The results obtained in this study indicate that antisera against E3-6-CMO-BSA, despite their appreciable cross-reaction with 6-oxoestriol, are as useful for a rapid RIA of plasma unconjugated E3 as antisera against E3-4-ABA-BSA because very little, if any, 6-oxoestriol is present in late pregnancy plasma. As anti-E3 titers were much higher and much more readily obtained in response to immunization with E3-6-CMO-BSA than with E3-4-ABA-BSA, E3-6-CMO-BSA appears to be the preferable antigen to develop antisera for a rapid, yet specific, E3 RIA.
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