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用于测量变应原特异性IgE和IgG抗体的酶联免疫吸附测定的放大。

Amplification of the enzyme-linked immunosorbent assay for measuring allergen-specific IgE and IgG antibody.

作者信息

Metzger W J, Butler J E, Swanson P, Reinders E, Richerson H B

出版信息

Clin Allergy. 1981 Nov;11(6):523-31. doi: 10.1111/j.1365-2222.1981.tb02170.x.

Abstract

The amplified enzyme-linked immunosorbent assay (a-ELISA) has been successfully applied to the measurement of allergen-specific IgE and IgG antibodies. Data presented indicate a high positive correlation among measurements of IgE-specific antibodies to ragweed antigen E using the a-ELISA, RAST and radiometric assay of Zeiss. Similarly, a high correlation between allergen-specific IgG antibodies measured by the a-ELISA and Farr assay was also observed. Data presented indicate that the measurement of serum IgE antibodies in the linear region of the ELISA titration plot is unaffected by competition with IgG antibodies. The assay is sensitive, reliable, and without risk to laboratory personnel. It is capable of measuring both IgE and IgG antibodies in patients using the same assay system.

摘要

扩增酶联免疫吸附测定(a-ELISA)已成功应用于过敏原特异性IgE和IgG抗体的检测。所呈现的数据表明,使用a-ELISA、放射性过敏原吸附试验(RAST)和蔡司放射测定法检测豚草抗原E特异性IgE抗体的结果之间存在高度正相关。同样,通过a-ELISA和法尔测定法检测的过敏原特异性IgG抗体之间也观察到高度相关性。所呈现的数据表明,在ELISA滴定图的线性区域测量血清IgE抗体不受与IgG抗体竞争的影响。该检测方法灵敏、可靠,对实验室人员无风险。它能够使用同一检测系统检测患者的IgE和IgG抗体。

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