水热
多重位移放大
热启动PCR
DNA聚合酶
分子生物学
底漆(化妆品)
聚合酶
DNA
生物
基因组DNA
聚合酶
重组酶聚合酶扩增
碱基对
PCR的应用
聚合酶链反应
聚合酶链反应优化
化学
底漆二聚体
遗传学
数字聚合酶链反应
多重聚合酶链反应
DNA提取
基因
有机化学
作者
Randall K. Saiki,David H. Gelfand,Susanne Stoffel,Stephen J. Scharf,Russell Higuchi,Glenn T. Horn,Kary B. Mullis,Henry A. Erlich
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1988-01-29
卷期号:239 (4839): 487-491
被引量:16971
标识
DOI:10.1126/science.2448875
摘要
A thermostable DNA polymerase was used in an in vitro DNA amplification procedure, the polymerase chain reaction. The enzyme, isolated from Thermus aquaticus, greatly simplifies the procedure and, by enabling the amplification reaction to be performed at higher temperatures, significantly improves the specificity, yield, sensitivity, and length of products that can be amplified. Single-copy genomic sequences were amplified by a factor of more than 10 million with very high specificity, and DNA segments up to 2000 base pairs were readily amplified. In addition, the method was used to amplify and detect a target DNA molecule present only once in a sample of 10(5) cells.
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