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通过梯度凝胶电泳分离血清高密度脂蛋白亚组分的直接定量分析。

Direct quantitation of serum high density lipoprotein subfractions separated by gradient gel electrophoresis.

作者信息

Gambert P, Farnier M, Bouzerand C, Athias A, Lallemant C

机构信息

Laboratoire de Biochimie Médicale, Faculté de Médecine, Dijon, France.

出版信息

Clin Chim Acta. 1988 Mar 15;172(2-3):183-90. doi: 10.1016/0009-8981(88)90322-1.

Abstract

This report describes the densitometric quantitation of the two main HDL subfractions separated by electrophoresis in a polyacrylamide gradient gel, HDLS (mean apparent diameter 9.3 nm) and HDLL (mean apparent diameter 10.6 nm). The electrophoresis was carried out in a linear gradient of polyacrylamide ranging from 23 to 180 g/l on total sera prestained for lipid components by Sudan black B in ethylene glycol. HDL subfractions were quantified by scanning the gels at 633 nm with a laser densitometer. The precision was checked by intra-assay and between-assay studies (coefficient of variation 1.2 and 2.9%, respectively). The results were compared with the cholesterol content of HDL subfractions (r = 0.99) and with the HDL2:HDL3 distribution (r = 0.95). Reference values were obtained from a population of 214 normolipidemic subjects. They were in good agreement with those already published for HDL2 and HDL3. The method which needs only 4 microliter of serum, can be set up with currently available apparatus and is compatible with large series of samples, should allow large scale explorations of the variation of HDL subfraction distribution in normal and pathological populations.

摘要

本报告描述了通过在聚丙烯酰胺梯度凝胶中进行电泳分离的两种主要高密度脂蛋白(HDL)亚组分的光密度定量分析,即HDLS(平均表观直径9.3纳米)和HDLL(平均表观直径10.6纳米)。电泳在聚丙烯酰胺线性梯度(范围为23至180克/升)中进行,样本为用乙二醇中的苏丹黑B对脂质成分进行预染色的全血清。通过用激光密度计在633纳米处扫描凝胶对HDL亚组分进行定量。通过批内和批间研究检查精密度(变异系数分别为1.2%和2.9%)。将结果与HDL亚组分的胆固醇含量进行比较(r = 0.99),并与HDL2:HDL3分布进行比较(r = 0.95)。参考值来自214名血脂正常受试者群体。它们与已发表的HDL2和HDL3参考值高度一致。该方法仅需4微升血清,可使用现有设备建立,且适用于大量样本,应能大规模探索正常和病理人群中HDL亚组分分布的变化情况。

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