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通过荧光原位杂交和流式细胞术测量端粒长度

Telomere length measurement by fluorescence in situ hybridization and flow cytometry.

作者信息

Kapoor Veena, Telford William G

机构信息

Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

出版信息

Methods Mol Biol. 2004;263:385-98. doi: 10.1385/1-59259-773-4:385.

DOI:10.1385/1-59259-773-4:385
PMID:14976379
Abstract

Telomere length is an important measure of cellular differentiation and progression to senescence. Flow cytometric assays for measuring telomere length have become an important adjunct to more laborious Southern blotting methods; telomere length can be estimated with considerable accuracy in small numbers of individual cells by flow cytometry, and can be measured in cell population subsets with simultaneous fluorescent immunophenotyping. In this chapter, we describe the standard flow cytometric assay for measuring telomere length, including the incorporation of fluorochrome-conjugated antibody immunolabeling for measurement in cell subsets.

摘要

端粒长度是细胞分化和衰老进程的一项重要指标。用于测量端粒长度的流式细胞术检测已成为更为繁琐的Southern印迹法的重要辅助手段;通过流式细胞术可以在少量单个细胞中相当准确地估计端粒长度,并且可以在进行同步荧光免疫表型分析的细胞群体亚群中进行测量。在本章中,我们描述了用于测量端粒长度的标准流式细胞术检测方法,包括使用荧光染料偶联抗体免疫标记来对细胞亚群进行测量。

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1
Telomere length measurement by fluorescence in situ hybridization and flow cytometry.通过荧光原位杂交和流式细胞术测量端粒长度
Methods Mol Biol. 2004;263:385-98. doi: 10.1385/1-59259-773-4:385.
2
Telomere length dynamics in human lymphocyte subpopulations measured by flow cytometry.通过流式细胞术测量人类淋巴细胞亚群中的端粒长度动态变化。
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Simultaneous flow cytometric analysis of two cell surface markers, telomere length, and DNA content.同时对两种细胞表面标志物、端粒长度和DNA含量进行流式细胞术分析。
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Flow cytometric analysis of fluorescence in situ hybridization with dye dilution and DNA staining (flow-FISH-DDD) to determine telomere length dynamics in proliferating cells.采用染料稀释和DNA染色的荧光原位杂交流式细胞术分析(流式荧光原位杂交-染料稀释和DNA染色法,flow-FISH-DDD)来确定增殖细胞中的端粒长度动态变化。
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Validation and development of quantitative flow cytometry-based fluorescence in situ hybridization for intercenter comparison of telomere length measurement.基于定量流式细胞术的荧光原位杂交技术用于端粒长度测量中心间比较的验证与开发
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Telomere length measurements in leukocyte subsets by automated multicolor flow-FISH.通过自动化多色流式荧光原位杂交技术测量白细胞亚群中的端粒长度
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Flow cytometry and FISH to measure the average length of telomeres (flow FISH).采用流式细胞术和荧光原位杂交技术来测量端粒的平均长度(流式荧光原位杂交技术)。
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Determination of telomere length by flow-fluorescence in situ hybridization in Down's syndrome patients.通过流式荧光原位杂交技术测定唐氏综合征患者的端粒长度。
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Comparison of different protocols for telomere length estimation by combination of quantitative fluorescence in situ hybridization (Q-FISH) and flow cytometry in human cancer cell lines.通过定量荧光原位杂交(Q-FISH)与流式细胞术相结合在人癌细胞系中估计端粒长度的不同方案比较。
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Abnormal telomerase activity and telomere length in T and B cells from patients with systemic lupus erythematosus.系统性红斑狼疮患者T细胞和B细胞中端粒酶活性及端粒长度异常。
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引用本文的文献

1
Assessment of Telomere Length, Phenotype, and DNA Content.端粒长度、表型及DNA含量的评估
Curr Protoc Cytom. 2017 Jan 5;79:7.26.1-7.26.23. doi: 10.1002/cpcy.12.
2
Direct comparison of flow-FISH and qPCR as diagnostic tests for telomere length measurement in humans.作为人类端粒长度测量诊断测试的流式荧光原位杂交技术(flow-FISH)和定量聚合酶链反应(qPCR)的直接比较。
PLoS One. 2014 Nov 19;9(11):e113747. doi: 10.1371/journal.pone.0113747. eCollection 2014.
3
Telomere DNA deficiency is associated with development of human embryonic aneuploidy.
端粒 DNA 缺陷与人类胚胎非整倍体的发生有关。
PLoS Genet. 2011 Jun;7(6):e1002161. doi: 10.1371/journal.pgen.1002161. Epub 2011 Jun 30.
4
Quantum dots thermal stability improves simultaneous phenotype-specific telomere length measurement by FISH-flow cytometry.量子点的热稳定性通过荧光原位杂交-流式细胞术改善了同时进行的表型特异性端粒长度测量。
J Immunol Methods. 2009 May 15;344(1):6-14. doi: 10.1016/j.jim.2009.02.004. Epub 2009 Mar 5.
5
Assessment of telomere length, phenotype, and DNA content.端粒长度、表型及DNA含量的评估。
Curr Protoc Cytom. 2004 Sep;Chapter 7:Unit 7.26. doi: 10.1002/0471142956.cy0726s29.