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采用非竞争性酶联免疫吸附测定法对人血浆载脂蛋白A-II进行定量测定。

Quantitative determination of human plasma apolipoprotein A-II by a non competitive enzyme-linked immunosorbent assay.

作者信息

Puchois P, Kandoussi A, Duriez P, Fruchart J C, McConathy W J, Koren E

出版信息

J Immunoassay. 1986;7(4):285-307. doi: 10.1080/01971528608060473.

Abstract

A noncompetitive enzyme-linked immunosorbent assay (ELISA) for apolipoprotein A-II (ApoA-II) was developed. Microtiter plates were coated with affinity purified antibodies to ApoA-II. After incubation with human plasma, the amount of ApoA-II bound to the coated plate was determined with peroxidase-labeled antibodies to ApoA-II. When pure ApoA-II or delipidated reference plasma was used as standard, a single step delipidation was required in order to unmask some antigenic sites of ApoA-II. However, the underestimated ApoA-II values in untreated samples were shown to be corrected by using intact reference plasma as secondary standard. The average concentration of ApoA-II in normolipidemic plasma was 0.376 g/l.

摘要

开发了一种用于载脂蛋白A-II(ApoA-II)的非竞争性酶联免疫吸附测定(ELISA)。微量滴定板用亲和纯化的抗ApoA-II抗体包被。与人血浆孵育后,用辣根过氧化物酶标记的抗ApoA-II抗体测定结合到包被板上的ApoA-II量。当使用纯ApoA-II或脱脂参考血浆作为标准品时,需要进行单步脱脂以暴露ApoA-II的一些抗原位点。然而,通过使用完整的参考血浆作为二级标准品,未处理样品中被低估的ApoA-II值被证明可以得到校正。正常血脂血浆中ApoA-II的平均浓度为0.376 g/l。

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