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快速循环和极端聚合酶链反应。

Rapid Cycle and Extreme Polymerase Chain Reaction.

机构信息

Crestwood Technology, Camden, ME, USA.

出版信息

Methods Mol Biol. 2023;2621:257-266. doi: 10.1007/978-1-0716-2950-5_14.

Abstract

Rapid cycle polymerase chain reaction (PCR) amplifies DNA in 10-30 min, while extreme PCR is complete in less than 1 min. These methods do not sacrifice quality for speed; sensitivity, specificity, and yield are equivalent or better than conventional PCR. What is required (and not widely available) is rapid, accurate control of reaction temperature during cycling. Specificity improves with cycling speed, and efficiency can be maintained by increasing polymerase and primer concentrations. Speed is aided by simplicity, dyes that stain double-stranded DNA are less expensive than probes, and one of the simplest polymerases, the deletion mutant KlenTaq, is used throughout. Rapid amplification can be coupled with endpoint melting analysis to verify product identity. Instead of commercial master mixes, detailed formulations for reagents and master mixes compatible with rapid cycle and extreme PCR are described.

摘要

快速循环聚合酶链反应 (PCR) 可在 10-30 分钟内扩增 DNA,而极端 PCR 可在不到 1 分钟内完成。这些方法不会为了速度而牺牲质量;灵敏度、特异性和产量与传统 PCR 相当或更好。需要的是(但并不广泛可用)在循环过程中快速、准确地控制反应温度。特异性随循环速度提高而提高,通过增加聚合酶和引物浓度可以保持效率。通过简单性来提高速度,而且由于双链 DNA 染色染料比探针便宜,因此使用最简单的聚合酶之一,缺失突变体 KlenTaq。快速扩增可以与终点熔解分析相结合,以验证产物的身份。本文介绍了与快速循环和极端 PCR 兼容的试剂和主混合物的详细配方,而不是商业主混合物。

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