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用于标记荧光核酸杂交探针的交互式荧光团和猝灭剂对。

Interactive fluorophore and quencher pairs for labeling fluorescent nucleic acid hybridization probes.

作者信息

Marras Salvatore A E

机构信息

Public Health Research Institute and the Department of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, 225 Warren Street, Newark, NJ, 07103, USA.

出版信息

Mol Biotechnol. 2008 Mar;38(3):247-55. doi: 10.1007/s12033-007-9012-9. Epub 2007 Nov 6.

Abstract

The use of fluorescent nucleic acid hybridization probes that generate a fluorescence signal only when they bind to their target enables real-time monitoring of nucleic acid amplification assays. Real-time nucleic acid amplification assays markedly improves the ability to obtain qualitative and quantitative results. Furthermore, these assays can be carried out in sealed tubes, eliminating carryover contamination. Fluorescent nucleic acid hybridization probes are available in a wide range of different fluorophore and quencher pairs. Multiple hybridization probes, each designed for the detection of a different nucleic acid sequence and each labeled with a differently colored fluorophore, can be added to the same nucleic acid amplification reaction, enabling the development of high-throughput multiplex assays. In order to develop robust, highly sensitive and specific real-time nucleic acid amplification assays it is important to carefully select the fluorophore and quencher labels of hybridization probes. Selection criteria are based on the type of hybridization probe used in the assay, the number of targets to be detected, and the type of apparatus available to perform the assay. This article provides an overview of different aspects of choosing appropriate labels for the different types of fluorescent hybridization probes used with different types of spectrofluorometric thermal cyclers currently available.

摘要

使用仅在与靶标结合时才产生荧光信号的荧光核酸杂交探针,能够对核酸扩增测定进行实时监测。实时核酸扩增测定显著提高了获得定性和定量结果的能力。此外,这些测定可以在密封管中进行,消除了交叉污染。荧光核酸杂交探针有多种不同的荧光团和猝灭剂对可供选择。可以将多个杂交探针添加到同一核酸扩增反应中,每个探针设计用于检测不同的核酸序列,并分别用不同颜色的荧光团标记,从而实现高通量多重测定的开发。为了开发稳健、高度灵敏和特异的实时核酸扩增测定,仔细选择杂交探针的荧光团和猝灭剂标记非常重要。选择标准基于测定中使用的杂交探针类型、要检测的靶标数量以及可用于进行测定的仪器类型。本文概述了为目前可用的不同类型的荧光分光光度热循环仪所使用的不同类型荧光杂交探针选择合适标记的不同方面。

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