Performing quantitative reverse-transcribed polymerase chain reaction experiments

被引:60
作者
Lutfalla, Georges [1 ]
Uze, Gilles [1 ]
机构
[1] Univ Montpellier 2, UMR 5124, CNRS, Montpellier 05, France
来源
DNA MICROARRAYS PART A: ARRAY PLATFORMS AND WET-BENCH PROTOCOLS | 2006年 / 410卷
关键词
D O I
10.1016/S0076-6879(06)10019-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitative polymerase chain reaction (PCR) is as old as PCR, but it has had to wait for the introduction of real-time PCR instruments to become widely used. These instruments allow monitoring of the PCR reaction on line; they involve the use of a fluorescent probe that allows quantification of the amplified DNA. Different fluorescent formats and different applications have been developed for quantitative PCR, but this chapter focuses on the use of the SYBR Green label for the quantification of specific cDNAs in reverse transcription mixes: RT-PCR. We propose optimal reaction conditions for the reactions to be performed on the different available instruments and discuss the important parameters for setting up experiments: specificity, efficiency, and reproducibility. We also introduce the reader to the problems of relative quantification.
引用
收藏
页码:386 / 400
页数:15
相关论文
共 15 条
[1]   Simplified hot start PCR [J].
Birch, DE ;
Kolmodin, L ;
Laird, WJ ;
McKinney, N ;
Wong, J ;
Young, KKY ;
Zangenberg, GA ;
Zoccoli, MA .
NATURE, 1996, 381 (6581) :445-446
[2]   PREVENTION OF PRE-PCR MIS-PRIMING AND PRIMER DIMERIZATION IMPROVES LOW-COPY-NUMBER AMPLIFICATIONS [J].
CHOU, Q ;
RUSSELL, M ;
BIRCH, DE ;
RAYMOND, J ;
BLOCH, W .
NUCLEIC ACIDS RESEARCH, 1992, 20 (07) :1717-1723
[3]   Viral infection and Toll-like receptor agonists induce a differential expression of type I and λ interferons in human plasmacytoid and monocyte-derived dendritic cells [J].
Coccia, EM ;
Severa, M ;
Giacomini, E ;
Monneron, D ;
Remoli, ME ;
Julkunen, I ;
Cella, M ;
Lande, R ;
Uzé, G .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2004, 34 (03) :796-805
[4]   Down-modulation of responses to type IIFN upon T cell activation [J].
Dondi, E ;
Rogge, L ;
Lutfalla, G ;
Uzé, G ;
Pellegrini, S .
JOURNAL OF IMMUNOLOGY, 2003, 170 (02) :749-756
[5]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[6]  
KELLOGG DE, 1994, BIOTECHNIQUES, V16, P1134
[7]   Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method [J].
Livak, KJ ;
Schmittgen, TD .
METHODS, 2001, 25 (04) :402-408
[8]   Comparative genomic analysis reveals independent expansion of a lineage-specific gene family in vertebrates: The class II cytokine receptors and their ligands in mammals and fish [J].
Lutfalla, G ;
Roest Crollius, H ;
Stange-thomann, N ;
Jaillon, O ;
Mogensen, K ;
Monneron, D .
BMC GENOMICS, 2003, 4 (1)
[9]  
NUOVO GJ, 1991, AM J PATHOL, V139, P1239
[10]   A new mathematical model for relative quantification in real-time RT-PCR [J].
Pfaffl, MW .
NUCLEIC ACIDS RESEARCH, 2001, 29 (09) :E45