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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Assembling long heteroduplexes by asymmetric polymerase chain reaction and annealing the resulting single-stranded DNAs
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Assembling long heteroduplexes by asymmetric polymerase chain reaction and annealing the resulting single-stranded DNAs

机译:通过不对称聚合酶链反应组装长异源双链并退火所得的单链DNA

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摘要

We developed an effective protocol for generating high-purity heteroduplexes via annealing single-stranded DNAs (ssDNAs) derived from plasmid DNA by asymmetric polymerase chain reaction (A-PCR). With the addition of dimethyl sulfoxide, a one-step A-PCR procedure can generate ssDNAs stably at a range of reaction temperatures. Several annealing buffers can anneal two ssDNAs into heteroduplexes effectively. We further developed a simple strategy to create d(GATC) hemimethylated heteroduplexes by annealing fully methylated homoduplexes in the presence of excessive unmethylated ssDNAs. The constructed heteroduplexes have been well tested as substrates for mismatch repair in Escherichia coli and, thus, can be used in various biotechnology applications. (C) 2015 Elsevier Inc. All rights reserved.
机译:我们开发了一种通过退火通过不对称聚合酶链反应(A-PCR)从质粒DNA衍生的单链DNA(ssDNA)来生成高纯度异源双链体的有效协议。通过添加二甲基亚砜,一步式A-PCR程序可以在一定的反应温度范围内稳定地生成ssDNA。几种退火缓冲液可以有效地将两个单链DNA退火为异源双链体。我们进一步开发了一种简单的策略,可以通过在存在过多未甲基化ssDNA的情况下对完全甲基化的同质双链进行退火来创建d(GATC)半甲基化的异双链。所构建的异源双链体已经过很好的测试,可作为大肠杆菌错配修复的底物,因此可用于各种生物技术应用中。 (C)2015 Elsevier Inc.保留所有权利。

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