多重位移放大
DNA聚合酶
滚动圆复制
DNA聚合酶Ⅱ
DNA钳
体外重组
生物
DNA纳米球测序
过程性
分子生物学
DNA聚合酶Ⅰ
聚合酶
PCR的应用
DNA
聚合酶链反应
基因组文库
遗传学
分子克隆
基因
多重聚合酶链反应
DNA提取
互补DNA
逆转录酶
基序列
作者
John Nelson,Yuyang Cai,Theresa L. Giesler,J. W. Farchaus,Shanmuuga T. Sundaram,María Ortiz-Rivera,Lou P. Hosta,Peter L. Hewitt,J. Anthony Mamone,Chockalingam Palaniappan,Carl W. Fuller
出处
期刊:BioTechniques
[Future Science Ltd]
日期:2002-06-01
卷期号:32 (sup6): 44-7
被引量:139
摘要
We have developed a novel, isothermal DNA amplification strategy that employs phi29 DNA polymerase and rolling circle amplification to generate high-quality templates for DNA sequencing reactions. The TempliPhi DNA amplification kits take advantage of the fact that cloned DNA is typically obtained in circular vectors, which are readily replicated in vitro using phi29 DNA polymerase by a rolling circle mechanism. This single subunit, proofreading DNA polymerase has excellent processivity and strand displacement properties for generation of multiple, tandem double-stranded copies of the circular DNA, generating as much as 10(7)-fold amplification. Large amounts of product (1-3 microg) can be obtained in as little as 4 hours. Input DNA can be as little as 0.01 ng of purified plasmid DNA, a single bacterial colony, or a 1 microL of a saturated overnight culture. Additionally, the presence of an associated proof reading function within the phi29 DNA polymerase ensures high-fidelity amplification. Once completed, the product DNA can be used directly in sequencing reactions. Additionally, the properties of phi29 DNA polymerase and its use in applications such as amplification ofhuman genomic DNA for genotyping studies is discussed.
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