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Immune cell subsets and their gene expression profiles from human PBMC isolated by Vacutainer Cell Preparation Tube (CPT™) and standard density gradient

机译:通过真空容器制备管(CPT™)和标准密度梯度分离的人PBMC的免疫细胞亚群及其基因表达谱

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摘要

BackgroundHigh quality genetic material is an essential pre-requisite when analyzing gene expression using microarray technology. Peripheral blood mononuclear cells (PBMC) are frequently used for genomic analyses, but several factors can affect the integrity of nucleic acids prior to their extraction, including the methods of PBMC collection and isolation. Due to the lack of the relevant data published, we compared the Ficoll-Paque density gradient centrifugation and BD Vacutainer cell preparation tube (CPT) protocols to determine if either method offered a distinct advantage in preparation of PBMC-derived immune cell subsets for their use in gene expression analysis. We evaluated the yield and purity of immune cell subpopulations isolated from PBMC derived by both methods, the quantity and quality of extracted nucleic acids, and compared gene expression in PBMC and individual immune cell types from Ficoll and CPT isolation protocols using Affymetrix microarrays.
机译:背景技术使用微阵列技术分析基因表达时,高质量的遗传物质是必不可少的前提。外周血单个核细胞(PBMC)通常用于基因组分析,但是在提取核酸之前,有几个因素会影响核酸的完整性,包括PBMC的收集和分离方法。由于缺乏相关数据,我们比较了Ficoll-Paque密度梯度离心和BD Vacutainer细胞制备管(CPT)方案,以确定这两种方法在制备PBMC衍生的免疫细胞亚群时是否具有明显的优势在基因表达分析中。我们评估了通过两种方法从PBMC中分离出的免疫细胞亚群的产量和纯度,提取核酸的数量和质量,并比较了PBMC中的基因表达以及使用Affymetrix微阵列从Ficoll和CPT分离方案得到的单个免疫细胞类型。

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