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Locked Nucleic Acid Flow Cytometry-fluorescence in situ Hybridization (LNA flow-FISH): a Method for Bacterial Small RNA Detection

机译:锁定核酸流式细胞术-荧光原位杂交(LNA流式-FISH):一种细菌小RNA检测方法

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摘要

Fluorescence in situ hybridization (FISH) is a powerful technique that is used to detect and localize specific nucleic acid sequences in the cellular environment. In order to increase throughput, FISH can be combined with flow cytometry (flow-FISH) to enable the detection of targeted nucleic acid sequences in thousands of individual cells. As a result, flow-FISH offers a distinct advantage over lysate/ensemble-based nucleic acid detection methods because each cell is treated as an independent observation, thereby permitting stronger statistical and variance analyses. These attributes have prompted the use of FISH and flow-FISH methods in a number of different applications and the utility of these methods has been successfully demonstrated in telomere length determination1,2, cellular identification and gene expression3,4, monitoring viral multiplication in infected cells5, and bacterial community analysis and enumeration6.
机译:荧光原位杂交(FISH)是一项功能强大的技术,可用于检测和定位细胞环境中的特定核酸序列。为了增加通量,可以将FISH与流式细胞仪(flow-FISH)结合使用,以检测成千上万个单个细胞中的目标核酸序列。结果,flow-FISH与基于裂解物/整体的核酸检测方法相比具有明显的优势,因为每个细胞都被视为独立的观察值,从而可以进行更强大的统计和方差分析。这些属性促使FISH和flow-FISH方法在许多不同的应用中得到使用,并且这些方法的效用已在端粒长度确定1,2,细胞鉴定和基因表达3,4,监测感染细胞中的病毒繁殖5中得到了成功证明5。以及细菌群落分析和枚举6。

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