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八个实验室间用于检测牛副结核病的一种商用酶联免疫吸附测定法的可重复性

Reproducibility of a commercial enzyme-linked immunosorbent assay for bovine paratuberculosis among eight laboratories.

作者信息

Collins M T, Angulo A, Buergelt C D, Hennager S G, Hietala S K, Jacobson R H, Whipple D L, Whitlock R H

机构信息

Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison 53706.

出版信息

J Vet Diagn Invest. 1993 Jan;5(1):52-5. doi: 10.1177/104063879300500112.

Abstract

Interlaboratory reproducibility of an absorbed enzyme-linked immunosorbent assay (ELISA) kit for detection of bovine serum antibodies to Mycobacterium paratuberculosis was evaluated. A panel of 30 bovine sera (15 positives and 15 negatives) was tested in triplicate microtiter wells on each of 2 days at 8 different laboratories. One laboratory had invalid results because of positive or negative serum control optical density (OD) readings beyond the acceptable range specified by the kit. The coefficient of variation (CV) for mean OD values was influenced by low ODs on test negative sera at 2 laboratories, thus the CVs on positive sera were considered a more representative measure of kit reproducibility. Between-well CVs averaged 6.7% +/- 2.8% (mean +/- standard deviation), and between-day CVs averaged 14.5% +/- 9.8% among the 7 laboratories with valid assays on the 15 positive sera. The OD values were converted to positive or negative classifications for each assay well, and the results were compared. Among 1,392 assays in 7 laboratories, 98.6% were in agreement. Eleven of 18 discrepant results were due to a sample that consistently gave OD values near the cutoff for a positive test. Exclusion of that serum from the analysis resulted in a 99.8% rate of agreement among laboratories. Results indicated that the absorbed ELISA kit provided reproducible results within and between laboratories.

摘要

对一种用于检测牛血清中副结核分枝杆菌抗体的吸收酶联免疫吸附测定(ELISA)试剂盒的实验室间再现性进行了评估。在8个不同实验室的每一个实验室中,将一组30份牛血清(15份阳性和15份阴性)在微量滴定孔中重复检测3次,共检测2天。有一个实验室的结果无效,因为阳性或阴性血清对照的光密度(OD)读数超出了试剂盒规定的可接受范围。平均OD值的变异系数(CV)受2个实验室检测阴性血清低OD值的影响,因此阳性血清的CV被认为是试剂盒再现性更具代表性的指标。在对15份阳性血清进行有效检测的7个实验室中,孔间CV平均为6.7%±2.8%(平均值±标准差),日间CV平均为14.5%±9.8%。将每个检测孔的OD值转换为阳性或阴性分类,并对结果进行比较。在7个实验室的1392次检测中,98.6%的结果一致。18个不一致结果中有11个是由于一个样本的OD值始终接近阳性检测的临界值。将该血清排除在分析之外后,实验室间的一致率达到99.8%。结果表明,该吸收ELISA试剂盒在实验室内部和实验室之间均能提供可重复的结果。

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