调解人
荧光团
化学
分子生物学
实时聚合酶链反应
核糖核酸
荧光
DNA
计算生物学
组合化学
寡核苷酸
核酸
生物
生物化学
细胞生物学
基因
量子力学
物理
作者
Simon Wadle,Stefanie Rubenwolf,Michael Lehnert,Bernd Faltin,Manfred Weidmann,Frank T. Hufert,Roland Zengerle,Felix von Stetten
标识
DOI:10.1007/978-1-4939-0733-5_6
摘要
Mediator probe PCR (MP PCR) is a novel detection format for real-time nucleic acid analysis. Label-free mediator probes (MP) and fluorogenic universal reporter (UR) oligonucleotides are combined to accomplish signal generation. Compared to conventional hydrolysis probe PCRs costs can thus be saved by using the same fluorogenic UR for signal generation in different assays. This tutorial provides a practical guideline to MP and UR design. MP design rules are very similar to those of hydrolysis probes. The major difference is in the replacement of the fluorophore and quencher by one UR-specific sequence tag, the mediator. Further protocols for the setup of reactions, to detect either DNA or RNA targets with clinical diagnostic target detection as models, are explained. Ready to use designs for URs are suggested and guidelines for their de novo design are provided as well, including a protocol for UR signal generation characterization.
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