Quantitative real-time RT-PCR - a perspective

被引:992
作者
Bustin, SA
Benes, V
Nolan, T
Pfaffl, MW
机构
[1] EMBL Heidelberg, D-69117 Heidelberg, Germany
[2] Stratagene Europe, NL-1100 AB Amsterdam, Netherlands
[3] Tech Univ Munich, Physiol Abt, Zent Inst Ernahrungs & Lebensmittelforsch, D-85354 Freising Weihenstephan, Germany
[4] Univ London, Barts & London Queen Marys Sch Med & Dent, Inst Cellular & Mol Sci, London, England
关键词
D O I
10.1677/jme.1.01755
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The real-time reverse transcription polymerase, chain reaction (RT-PCR) uses fluorescent reporter molecules to monitor the production of amplification products during each cycle of the PCR reaction. This combines the nucleic acid amplification and detection steps into one homogeneous assay and obviates the need for gel electrophoresis to detect amplification products. Use of appropriate chemistries and data analysis eliminates the need for Southern blotting or DNA sequencing for amplicon identification. Its simplicity, specificity and sensitivity, together with its potential for high throughput and the ongoing introduction of new chemistries, more reliable instrumentation and improved protocols, has made real-time RT-PCR the benchmark technology for the detection and/or comparison of RNA levels.
引用
收藏
页码:597 / 601
页数:5
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