Detection of PCR products using self-probing amplicons and fluorescence

被引:506
作者
Whitcombe, D
Theaker, J
Guy, SP
Brown, T
Little, S
机构
[1] AstraZeneca Diagnost, Northwich CW9 7RA, Cheshire, England
[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England
关键词
homogeneous assays; fluorescent probes; diagnostics; PCR; ARMS; single-tube genotyping; multiplexing;
D O I
10.1038/11751
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molecular diagnostics is progressing from low-throughput, heterogeneous, mostly manual technologies to higher throughput, closed-tube, and automated methods. Fluorescence is the favored signaling technology for such assays, and a number of techniques rely on energy transfer between a fluorophore and a proximal quencher molecule, In these methods, dual-labeled probes hybridize to an amplicon and changes in the quenching of the fluorophore are detected. We describe a new technology that is simple to use, gives highly specific information, and avoids the major difficulties of the alternative methods, It uses a primer with an integral tail that is used to probe an extension product of the primer, The probing of a target sequence is thereby converted into a unimolecular event, which has substantial benefits in terms of kinetics, thermodynamics, assay design, and probe reliability.
引用
收藏
页码:804 / 807
页数:4
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