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用于检测曼氏血吸虫抗体的快速酶联免疫吸附测定法的开发与优化

Development and optimization of the FAST-ELISA for detecting antibodies to Schistosoma mansoni.

作者信息

Hancock K, Tsang V C

出版信息

J Immunol Methods. 1986 Sep 27;92(2):167-76. doi: 10.1016/0022-1759(86)90162-6.

Abstract

The Falcon assay screening test (F.A.S.T.) system was used to develop a rapid, sensitive, and quantitative kinetic-based enzyme-linked immunosorbent assay (k-ELISA) for detecting antibodies against Schistosoma mansoni adult microsomal antigens (MAMAs). The FAST-ELISA uses polystyrene beads on sticks molded to the lid of a microtitration plate. The beads are coated with antigen. Reagents and sera are placed in microtitration plates and the beads exposed to reagents by immersion. The exposure time required for a single dilution of serum or other antibody source, conjugate, and substrate is 5 min each. Excluding preparation time, two plates can easily be assayed in 30 min. The optima for assay conditions, reproducibility, quantitative linearity, and sensitivity are delineated. A battery of sera from patients with both homologous and heterologous infections was tested, and a dilution series of a standard reference serum pool was included with each test. Results were expressed in number of units as calibrated against the standard reference sera pool. Antigen-coated bead storage studies were performed with untreated and three chemically treated antigens. The storage stability of MAMA, ability to perform the assay with minimal equipment, sensitivity, short assay time, and ease of operation make the FAST-ELISA ideal for field studies.

摘要

采用Falcon分析筛选试验(F.A.S.T.)系统开发了一种基于动力学的快速、灵敏且定量的酶联免疫吸附测定法(k-ELISA),用于检测抗曼氏血吸虫成虫微粒体抗原(MAMA)的抗体。快速酶联免疫吸附测定法(FAST-ELISA)使用模制在微量滴定板盖上的棒上的聚苯乙烯珠。珠子包被有抗原。将试剂和血清置于微量滴定板中,通过浸泡使珠子接触试剂。血清或其他抗体来源、结合物和底物单次稀释所需的接触时间均为5分钟。不包括准备时间,30分钟内可轻松检测两块板。确定了测定条件、重现性、定量线性和灵敏度的最佳参数。检测了一组同源和异源感染患者的血清,并在每次检测中纳入标准参考血清库的稀释系列。结果以相对于标准参考血清库校准的单位数表示。对未处理的和三种化学处理的抗原进行了包被抗原的珠子储存研究。MAMA的储存稳定性、使用最少设备进行测定的能力、灵敏度、短测定时间和易于操作使FAST-ELISA成为现场研究的理想选择。

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