Quantitation of viral load using real-time amplification techniques

被引:188
作者
Niesters, HGM [1 ]
机构
[1] Univ Rotterdam Hosp, Dept Virol, NL-3015 GD Rotterdam, Netherlands
关键词
quantitative techniques; real-time technology; polymerase chain reaction; nucleic sequence-based amplification; molecular beacons; hydrolysis probes; TaqMan technology; hybridization probes; standardization;
D O I
10.1006/meth.2001.1264
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Real-time PCR amplification techniques are currently used to determine the viral load in clinical samples for an increasing number of targets. Real-time PCR reduces the time necessary to generate results after amplification. In-house developed PCR and nucleic acid sequence-based amplification (NASBA)-based systems combined with several detection strategies are being employed in a clinical diagnostic setting. The importance of these assays in disease management Is still In an exploration phase. Although these technologies have the implicit capability of accurately measuring DNA and RNA In clinical samples, issues related to standardization and quality control must be resolved to enable routine implementation of these technologies in molecular diagnostics. (C) 2001 Elsevier Science (USA).
引用
收藏
页码:419 / 429
页数:11
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