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Comparative analysis of EV isolation procedures for miRNAs detection in serum samples

机译:用于血清样品中miRNA检测的EV分离程序的比较分析

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Extracellular vesicles (EVs) are emerging as potent non-invasive biomarkers. However, current methodologies are time consuming and difficult to translate to clinical practice. To analyse EV-encapsulated circulating miRNA, we searched for a quick, easy and economic method to enrich frozen human serum samples for EV. We compared the efficiency of several protocols and commercial kits to isolate EVs. Different methods based on precipitation, columns or filter systems were tested and compared with ultracentrifugation, which is the most classical protocol to isolate EVs. EV samples were assessed for purity and quantity by nanoparticle tracking analysis and western blot or cytometry against major EV protein markers. For biomarker validation, levels of a set of miRNAs were determined in EV fractions and compared with their levels in total serum. EVs isolated with precipitation-based methods were enriched for a subgroup of miRNAs that corresponded to miRNAs described to be encapsulated into EVs (miR-126, miR-30c ...
机译:细胞外囊泡(EVs)新兴成为有效的非侵入性生物标志物。然而,当前的方法学很耗时并且难以转化为临床实践。为了分析EV封装的循环miRNA,我们寻找一种快速,简便且经济的方法来富集冷冻人血清样品中的EV。我们比较了几种协议和商业套件隔离电动汽车的效率。测试了基于沉淀,色谱柱或过滤器系统的不同方法,并将其与超离心分离进行了比较,超离心是分离电动汽车的最经典方法。通过纳米颗粒追踪分析和针对主要EV蛋白标志物的Western印迹或细胞计数法评估EV样品的纯度和数量。为了验证生物标志物,在EV馏分中确定了一组miRNA的水平,并将其与总血清中的水平进行比较。用基于沉淀的方法分离出的EV丰富了miRNA的一个亚组,该亚组对应于被描述为封装在EV中的miRNA(miR-126,miR-30c ...

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