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[运用单克隆抗体在非竞争性酶联免疫吸附测定法中对血清载脂蛋白AI进行定量测定]

[Quantitative determination of apolipoprotein AI in serum by the use of monoclonal antibodies in a noncompetitive ELISA].

作者信息

Winkler L, Müller D W, Dargel R, Jäger L

机构信息

Institut für Pathologische Biochemie, Friedrich-Schiller-Universität Jena.

出版信息

Z Med Lab Diagn. 1990;31(3):159-64.

PMID:2114707
Abstract

A methodical base for estimation of apolipoprotein AI (apo AI) in the serum using a monoclonal antibody in a non-competitive ELISA is described. The technical approach is adjusted to commercial materials of the DDR industry. The assay allows to determine apo AI within the range of 5-100 micrograms apo AI/I. The Vk was 4% (within), and 8% (day to day). The monoclonal antibody used is directed against a native epitope which is fully exposed in the serum. Application of the SUMAL system further improves the practicability of the method. The assay should be suitable particularly for the recognition of epitopes of apo AI in serum HDL fractions associated with an atherogenic risk. The values obtained by the ELISA correspond to those measured turbidimetrically using polyclonal antibodies.

摘要

描述了一种在非竞争性酶联免疫吸附测定(ELISA)中使用单克隆抗体测定血清中载脂蛋白AI(apo AI)的系统方法。该技术方法已根据民主德国工业的商业材料进行了调整。该测定法可测定5 - 100微克apo AI/I范围内的apo AI。批内变异系数为4%,批间变异系数为8%。所使用的单克隆抗体针对血清中完全暴露的天然表位。SUMAL系统的应用进一步提高了该方法的实用性。该测定法尤其适用于识别与动脉粥样硬化风险相关的血清高密度脂蛋白(HDL)组分中apo AI的表位。ELISA法获得的值与使用多克隆抗体通过比浊法测得的值一致。

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