Real-time turbidimetry of LAMP reaction for quantifying template DNA

被引:503
作者
Mori, Y [1 ]
Kitao, M [1 ]
Tomita, N [1 ]
Notomi, T [1 ]
机构
[1] Eiken Chem Co Ltd, Biochem Res Lab, Ohtawara, Tochigi 3240036, Japan
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2004年 / 59卷 / 02期
关键词
loop-mediated isothermal amplification; LAMP; real-time turbidimetry; quantification of template;
D O I
10.1016/j.jbbm.2003.12.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Loop-mediated isothermal amplification (LAMP) is a nucleic acid amplification method that allows the synthesis of large amounts of DNA in a short period of time with high specificity. As the LAMP reaction progresses, the reaction by-product pyrophosphate ions bind to magnesium ions and form a white precipitate of magnesium pyrophosphate. We designed an apparatus capable of measuring the turbidity of multiple samples simultaneously while maintaining constant temperature to conduct real-time measurements of the changes in the turbidity of LAMP reactions. The time (T,) required for the turbidity of the LAMP reaction solution to exceed a given value was dependent on the quantity of the initial template DNA. That is, a graph with the plot of T-t versus the log of the amount of initial template DNA was linear from 2 x 10(3) copies (0.01 pg/tube) to 2 x 10(9) copies (100 ng/tube) of template DNA. These results indicate that real-time turbidity measurements of the LAMP reaction permit the quantitative analysis of minute amounts of nucleic acids present in a sample, with a high precision over a wide range, using a simple apparatus reported in this study. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:145 / 157
页数:13
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