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首页> 外文期刊>Journal of Immunological Methods >The modified FACS calcein AM retention assay: A high throughput flow cytometer based method to measure cytotoxicity
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The modified FACS calcein AM retention assay: A high throughput flow cytometer based method to measure cytotoxicity

机译:改进的FACS钙黄绿素AM保留测定法:一种基于高通量流式细胞仪的细胞毒性测量方法

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摘要

Current methods to determine cellular cytotoxicity in vitro are hampered by background signals that are caused by auto-fluorescent target and effector cells and by non-specific cell death. We combined and adjusted existing cell viability assays to develop a method that allows for highly reproducible, accurate, single cell analysis by high throughput FACS, in which non-specific cell death is corrected for. In this assay the number of living, calcein AM labeled cells that are green fluorescent are quantified by adding a fixed number of unlabeled calibration beads to the analysis. Using this modified FACS calcein AM retention method, we found EC50 values to be highly reproducible and considerably lower compared to EC50 values obtained by conventional assays, displaying the high sensitivity of this assay. (C) 2016 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
机译:当前确定体外细胞毒性的方法受到背景信号的影响,这些背景信号是由自发荧光的靶细胞和效应细胞以及非特异性细胞死亡引起的。我们结合并调整了现有的细胞生存力检测方法,以开发一种方法,该方法可通过高通量FACS进行高度可重复,准确,单细胞分析,从而纠正了非特异性细胞死亡。在该测定中,通过向分析中添加固定数量的未标记校准珠,可以定量检测绿色荧光的活的钙黄绿素AM标记的活细胞的数量。使用这种改良的FACS钙黄绿素AM保留方法,我们发现EC50值具有很高的重现性,并且与通过常规测定获得的EC50值相比,其值要低得多,显示出该测定法的高灵敏度。 (C)2016作者。由Elsevier B.V.发布。这是CC BY-NC-ND许可(http://creativecommons.org/licenses/by-nc-nd/4.0/)下的开放获取文章。

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