首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Cell phenotype analysis using a cell fluid-based microchip wit high sensitivity and accurate quantitation
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Cell phenotype analysis using a cell fluid-based microchip wit high sensitivity and accurate quantitation

机译:使用基于细胞液的微芯片具有高灵敏度和准确定量的细胞表型分析

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We have assessed a cell fluid chip-based fluorescent cytometric assay that runs on bioanalyzer for fast characterization of small population cell phenotypes characterization. The assay determines the expression of specific cell surface markers on various cell samples. Six samples can be analyzed on each chip in one automated process. Results were in good agreement with conventional flow cytometry in quantitation. Importantly, this procedure used less than 200 cells per sample and produced results consistent with that using 10~5 cells by the conventional staining procedure. The method was also used for screening potential ingredients in herbs. Purpose of this study was to analyze the change of cell subtypes of UCB mononuclear cells in vitro reactivity in herbs. We found that by treatment of the water-soluble extract (F3) of Ganoderma lucidum, the presence of CD56~+ marker (natural killer cells) significantly increased from 1.1 to 3.2% (P < 0.05 and P) in UCB mononuclear cells. The results indicated that F3 quantitatively influenced NK cells activities. We suggest this screening method may be useful for a fast phenotypes characterization after extract stimulation utilizing only a small population of cells.
机译:我们评估了基于细胞液芯片的荧光细胞计数分析,该分析在生物分析仪上运行,可快速表征小群体细胞表型。该测定法确定各种细胞样品上特异性细胞表面标志物的表达。在一个自动化过程中,可以在每个芯片上分析六个样品。结果与定量的常规流式细胞仪非常吻合。重要的是,该程序每个样品使用少于200个细胞,产生的结果与常规染色程序使用10〜5个细胞的结果一致。该方法还用于筛选草药中的潜在成分。这项研究的目的是分析草药中UCB单核细胞体外反应性的细胞亚型的变化。我们发现,通过处理灵芝的水溶性提取物(F3),UCB单核细胞中CD56〜+标记(自然杀伤细胞)的存在从1.1%显着增加到3.2%(P <0.05和P)。结果表明F3定量影响NK细胞活性。我们建议这种筛选方法可能对仅利用少量细胞的提取物刺激后的快速表型表征有用。

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