首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Single-spin density-gradient ultracentrifugation vs gradient gel electrophoresis: two methods for detecting low-density-lipoprotein heterogeneity compared.
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Single-spin density-gradient ultracentrifugation vs gradient gel electrophoresis: two methods for detecting low-density-lipoprotein heterogeneity compared.

机译:单旋密度梯度超速离心与梯度凝胶电泳:两种检测低密度脂蛋白异质性的方法进行了比较。

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Single-spin density-gradient ultracentrifugation (DUC) has proven to be a reproducible method for detection of low-density-lipoprotein (LDL) heterogeneity. Recently another method has been described for this: gradient gel electrophoresis (GGE) of serum, a method that might be more suitable for screening. To gain insight into the relationship of GGE to DUC and into their reproducibility, we determined LDL heterogeneity by DUC and GGE in 41 healthy individuals. In 90.2% (n = 37) of the subjects, the number of LDL subfractions found by both methods agreed. In addition, the density and the relative migration distance of the predominant LDL subfraction observed with the respective methods showed a strong correlation (Pearson correlation, r = 0.85, P less than 0.0001). Although it was not possible to compare for all aspects of LDL heterogeneity, these data suggest that GGE is a valid method of analysis for LDL heterogeneity. In screening programs, it may be necessary to store samples. Therefore, we studied in 24 sera the influence of storage at -80 degrees C for one, four, and 12 weeks on the LDL subfraction distribution detected by each method. LDL heterogeneity was maintained during storage under these conditions.
机译:单旋转密度梯度超速离心(DUC)已被证明是检测低密度脂蛋白(LDL)异质性的可重复方法。最近,已经对此进行了另一种描述:血清的梯度凝胶电泳(GGE),该方法可能更适合于筛选。为了深入了解GGE与DUC的关系及其可重复性,我们通过DUC和GGE在41位健康个体中确定了LDL异质性。在90.2%(n = 37)的受试者中,通过两种方法发现的LDL亚组分的数量均相符。此外,用相应方法观察到的主要LDL亚组分的密度和相对迁移距离显示出很强的相关性(Pearson相关性,r = 0.85,P小于0.0001)。尽管不可能对LDL异质性的所有方面进行比较,但这些数据表明GGE是分析LDL异质性的有效方法。在筛选程序中,可能需要存储样品。因此,我们在24个血清中研究了在-80摄氏度下储存1、4和12周对每种方法检测到的LDL亚组分分布的影响。在这些条件下的存储过程中,LDL异质性得以维持。

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