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
相关论文
共 38 条
[1]   Customized molecular phenotyping by quantitative gene expression and pattern recognition analysis [J].
Akilesh, S ;
Shaffer, DJ ;
Roopenian, D .
GENOME RESEARCH, 2003, 13 (07) :1719-1727
[2]   Normalization of real-time quantitative reverse transcription-PCR data: A model-based variance estimation approach to identify genes suited for normalization, applied to bladder and colon cancer data sets [J].
Andersen, CL ;
Jensen, JL ;
Orntoft, TF .
CANCER RESEARCH, 2004, 64 (15) :5245-5250
[3]   Utility of the housekeeping genes 18S rRNA, β-actin and glyceraldehyde-3-phosphate-dehydrogenase for normalization in real-time quantitative reverse transcriptase-polymerase chain reaction analysis of gene expression in human T lymphocytes [J].
Bas, A ;
Forsberg, G ;
Hammarström, S ;
Hammarström, ML .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2004, 59 (06) :566-573
[4]   COMPARISON OF GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE AND 28S-RIBOSOMAL RNA GENE-EXPRESSION AS RNA LOADING CONTROLS FOR NORTHERN BLOT ANALYSIS OF CELL-LINES OF VARYING MALIGNANT POTENTIAL [J].
BHATIA, P ;
TAYLOR, WR ;
GREENBERG, AH ;
WRIGHT, JA .
ANALYTICAL BIOCHEMISTRY, 1994, 216 (01) :223-226
[5]  
Bustin S. A., 2004, A Z QUANTITATIVE PCR
[6]   Detection of cytokeratins 19/20 and guanylyl cyclase C in peripheral blood of colorectal cancer patients [J].
Bustin, SA ;
Gyselman, VG ;
Williams, NS ;
Dorudi, S .
BRITISH JOURNAL OF CANCER, 1999, 79 (11-12) :1813-1820
[7]   Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays [J].
Bustin, SA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 25 (02) :169-193
[8]   Quantification of mRNA using real-time reverse transcription PCR (RT-PCR): trends and problems [J].
Bustin, SA .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2002, 29 (01) :23-39
[9]  
Bustin Stephen A, 2004, J Biomol Tech, V15, P155
[10]   Low efficiency of the Moloney murine leukemia virus reverse transcriptase during reverse transcription of rare t(8;21) fusion gene transcripts [J].
Curry, J ;
McHale, C ;
Smith, MT .
BIOTECHNIQUES, 2002, 32 (04) :768-+