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用于提高PCR扩增特异性和灵敏度的降落PCR。

Touchdown PCR for increased specificity and sensitivity in PCR amplification.

作者信息

Korbie Darren J, Mattick John S

机构信息

Australian Research Council Special Research Centre for Functional and Applied Genomics, Institute for Molecular Bioscience, University of Queensland, St Lucia, Queensland 4072, Australia.

出版信息

Nat Protoc. 2008;3(9):1452-6. doi: 10.1038/nprot.2008.133.

Abstract

Touchdown (TD) PCR offers a simple and rapid means to optimize PCRs, increasing specificity, sensitivity and yield, without the need for lengthy optimizations and/or the redesigning of primers. TD-PCR employs an initial annealing temperature above the projected melting temperature (T(m)) of the primers being used, then progressively transitions to a lower, more permissive annealing temperature over the course of successive cycles. Any difference in T(m) between correct and incorrect annealing will produce an exponential advantage of twofold per cycle. TD-PCR has found wide applicability in standard PCR protocols, including reverse transcriptase-dependent PCR, as well as in the generation of cDNA libraries and single nucleotide polymorphism screening. TD-PCR is particularly useful for templates that are difficult to amplify but can also be standardly used to enhance specificity and product formation. The procedure takes between 90 and 120 min, depending on the template length.

摘要

着陆式(TD)PCR提供了一种简单快速的方法来优化PCR,可提高特异性、灵敏度和产量,而无需进行冗长的优化和/或重新设计引物。TD-PCR采用高于所用引物预计解链温度(T(m))的初始退火温度,然后在连续循环过程中逐步过渡到较低、更宽松的退火温度。正确退火和错误退火之间的T(m)差异将在每个循环中产生两倍的指数优势。TD-PCR已在标准PCR方案中得到广泛应用,包括依赖逆转录酶的PCR,以及在cDNA文库的构建和单核苷酸多态性筛选中。TD-PCR对于难以扩增的模板特别有用,但也可常规用于提高特异性和产物形成。该过程需要90至120分钟,具体取决于模板长度。

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