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首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >NOVEL FLOW CYTOMETRIC METHOD FOR QUANTIFYING NUCLEAR BINDING OF THE TRANSCRIPTION FACTOR NUCLEAR FACTOR KAPPA B IN UNSEPARATED HUMAN MONOCYTES AND POLYMORPHONUCLEAR CELLS
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NOVEL FLOW CYTOMETRIC METHOD FOR QUANTIFYING NUCLEAR BINDING OF THE TRANSCRIPTION FACTOR NUCLEAR FACTOR KAPPA B IN UNSEPARATED HUMAN MONOCYTES AND POLYMORPHONUCLEAR CELLS

机译:定量分离人单核细胞和多聚核细胞中转录因子核因子κB的核结合的新型流式细胞术

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摘要

The transcription factor nuclear factor kappa B (NF kappa B) regulates the production of a number of pro-inflammatory mediators involved in polymorphonuclear and mononuclear cell activation. Measurement of NF kappa B DNA binding is used as an estimate of cellular activation and is usually measured by the DNA mobility shift assay. Results from the mobility shift assay can be difficult. to quantify and do not allow discrimination of activity in different populations of cells in whole blood without prior separation, This paper describes a new flow cytometric method which allows rapid detection and quantification of DNA-bound NP kappa B in white cell populations of whole blood. The technique is sensitive and allows discriminate analysis and quantification of bound NF kappa B in nuclei from polymorphonuclear and mononuclear ceh populations in whole blood. (C) 1997 Wiley-Liss, Inc. [References: 12]
机译:转录因子核因子κB(NFκB)调节参与多形核和单核细胞活化的多种促炎性介质的产生。 NF kappa B DNA结合的测量被用作细胞激活的评估,通常通过DNA迁移率变动分析进行测量。迁移率变动分析的结果可能很困难。为了定量分析并且不允许在没有事先分离的情况下区分全血中不同细胞群体的活性,本文描述了一种新的流式细胞术方法,该方法可以快速检测和定量全血白细胞群体中与DNA结合的NP kappaB。该技术非常灵敏,可以从全血中的多形核和单核ceh种群中区分出核中结合的NF kappa B的分析和定量。 (C)1997 Wiley-Liss,Inc. [参考:12]

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