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用于放射免疫分析的IgG在共价连接到氨基二乙氨基乙基纤维素珠上的第二抗体上的免疫吸附。

Immunoadsorption of IgG onto second antibody covalently attached to Amino-Dylark beads for radioimmunoassays.

作者信息

Kakabakos S E, Evangelatos G P, Ithakissios D S

机构信息

National Center for Scientific Research Demokritos, Athens, Greece.

出版信息

Clin Chem. 1990 Mar;36(3):497-500.

PMID:2178802
Abstract

We present a solid-phase immobilization method for radioligand assays, using an immunoadsorption coating procedure of anti-triiodothyronine rabbit IgG (anti-T3 IgG) onto second antibody (sheep anti-rabbit IgG) covalently bound to Amino-Dylark beads. The second antibody was in excess, compared with the first antibody, thus eliminating reproducibility problems between immunoadsorptions. Beads coated with second antibody can be used to immobilize a variety of antigen-specific first antibodies. The amount of anti-T3 antibody required for solid-phase T3 radioimmunoassay (RIA) was only 10% more, per assay tube, than that utilized in liquid-phase T3 RIA, in which polyethylene glycol solution was the separation reagent; characteristics of assay performance were comparable. The immobilization procedure requires high-titer antisera or antigen-specific IgG and seems advantageous because of the decrease in antibody requirements without significant modification of antibody functionality.

摘要

我们提出了一种用于放射性配体分析的固相固定方法,该方法采用将抗三碘甲状腺原氨酸兔免疫球蛋白G(抗T3 IgG)通过免疫吸附包被程序固定到与氨基-Dylark珠共价结合的第二抗体(羊抗兔IgG)上。与第一抗体相比,第二抗体过量,从而消除了免疫吸附之间的重现性问题。包被有第二抗体的珠子可用于固定多种抗原特异性第一抗体。固相T3放射免疫分析(RIA)每测定管所需的抗T3抗体量仅比以聚乙二醇溶液为分离试剂的液相T3 RIA多10%;分析性能特征相当。固定程序需要高滴度抗血清或抗原特异性IgG,并且由于抗体需求量减少而抗体功能无明显改变,似乎具有优势。

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