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血清中β2微球蛋白荧光免疫测定法的研制

The development of a fluoroimmunoassay for beta-2-microglobulin in serum.

作者信息

Playford R J, Dawnay A, Cattell W R, Landon J

出版信息

Ann Clin Biochem. 1985 Mar;22 ( Pt 2):166-70. doi: 10.1177/000456328502200211.

Abstract

A liquid-phase fluoroimmunoassay has been developed for the measurement of beta-2-microglobulin in undiluted serum or plasma. Protein labelled with fluorescein-isothiocyanate at a molar ratio of 1:2 respectively is employed as a tracer together with an antiserum to beta-2-microglobulin raised in a sheep. Separation is achieved by means of rabbit anti-sheep immunoglobulin G and, following precipitation of the bound fraction by centrifugation, the free fraction together with any potentially interfering factors is removed in the supernatant. Finally the precipitate is dissolved and the fluorescence measured. The assay is simple and rapid in that all reactants, including the second antibody, can be added at the start of the assay and equilibrium is attained within 60 min. The assay is reproducible and sufficiently sensitive to allow measurement of normal serum levels and has a wide range avoiding the need for sample dilution. Results correlated well with those of an established radioimmunoassay.

摘要

已开发出一种液相荧光免疫测定法,用于测定未稀释血清或血浆中的β2微球蛋白。分别以1:2的摩尔比用异硫氰酸荧光素标记的蛋白质用作示踪剂,同时使用在绵羊体内产生的抗β2微球蛋白抗血清。通过兔抗绵羊免疫球蛋白G实现分离,在通过离心沉淀结合部分后,将游离部分以及任何潜在干扰因素在上清液中去除。最后将沉淀物溶解并测量荧光。该测定法简单快速,因为所有反应物,包括第二抗体,都可以在测定开始时加入,并且在60分钟内达到平衡。该测定法具有可重复性且足够灵敏,能够测量正常血清水平,并且范围广泛,无需样品稀释。结果与既定的放射免疫测定法的结果相关性良好。

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