Influence of reagents formulation on real-time PCR parameters

被引:29
作者
Burgos, JS [1 ]
Ramírez, C [1 ]
Tenorio, R [1 ]
Sastre, I [1 ]
Bullido, MJ [1 ]
机构
[1] Univ Autonoma Madrid, Ctr Biol Mol Severo Ochoa, CSIC, Fac Sci,CX Lab 340, E-28049 Madrid, Spain
关键词
real-time PCR; SYBR Green I dye; beta-actin; DNA polymerase; glycoprotein B; thimidine kinase;
D O I
10.1006/mcpr.2002.0419
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Real-time polymerase chain reaction (PCR) techniques are increasingly used to quantify target sequences for diagnostic and research purposes. Due to its 'quantitative' character, it is very important to determine the variability of this technique correlating with several experimental conditions. The objective of this study was to analyse the effect of manufacturing lots of PCR reagents on two main PCR parameters, specificity and sensitivity. For this study, we used four different amplicons, using either mouse genomic DNA or viral DNA. Although a PCR product could be obtained in any of the conditions, we observed that there are relevant variations in sensitivity depending on the reagents formulation. We conclude that different lots of reagents may determine the analytical performance of PCR assays indicating that reagents testing are of special importance when the PCR protocol is used for quantitative purposes. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:257 / 260
页数:4
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