核酸
浊度法
浊度
化学
环介导等温扩增
镁
DNA
焦磷酸盐
色谱法
分析化学(期刊)
生物化学
有机化学
生物
生态学
酶
作者
Yasuyoshi Mori,Masataka Kitao,Norihiro Tomita,Tsugunori Notomi
出处
期刊:Journal of Biochemical and Biophysical Methods
[Elsevier BV]
日期:2004-05-01
卷期号:59 (2): 145-157
被引量:553
标识
DOI:10.1016/j.jbbm.2003.12.005
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 (Tt) 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 Tt 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.
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