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Titlebook: Rapid Cycle Real-Time PCR; Methods and Applicat Stefan Meuer,Carl Wittwer,Kan-Ichi Nakagawara Book 2001 Springer-Verlag Berlin Heidelberg 2

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書(shū)目名稱Rapid Cycle Real-Time PCR
副標(biāo)題Methods and Applicat
編輯Stefan Meuer,Carl Wittwer,Kan-Ichi Nakagawara
視頻videohttp://file.papertrans.cn/822/821175/821175.mp4
圖書(shū)封面Titlebook: Rapid Cycle Real-Time PCR; Methods and Applicat Stefan Meuer,Carl Wittwer,Kan-Ichi Nakagawara Book 2001 Springer-Verlag Berlin Heidelberg 2
描述The first comprehensive treatise on Rapid Cycle Real-Time PCR. With amplification times of 15-30 minutes of on-line detection and analysis, nucleic acid quantification of mutation analysis finally becomes a routine, powerful and rapid method. Focusing primarily on the LightCycler, an instrument that combines Rapid Cycle PCR with fluorescent monitoring, this technology provides convenient analysis by melting temperatures. PCR products can be identified by product Tm, and single base mismatches can easily be genotyped by probe Tm. Methods chapters detail the theory behind quantification of mutation analysis; the design of synthesis of fluorescent hybridization probes of the preparation of template DNA. Application chapters apply nucleid acid quantification to infectious organisms of intracellular messengers and mutation detection to somatic of acquired mutations.
出版日期Book 2001
關(guān)鍵詞DNA-/RNA-Diagnostik; PCR; T cell; antibody; cancer; chromosome; cytokine; gene analysis; genome; hemochromato
版次1
doihttps://doi.org/10.1007/978-3-642-59524-0
isbn_ebook978-3-642-59524-0
copyrightSpringer-Verlag Berlin Heidelberg 2001
The information of publication is updating

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nucleic acid quantification of mutation analysis finally becomes a routine, powerful and rapid method. Focusing primarily on the LightCycler, an instrument that combines Rapid Cycle PCR with fluorescent monitoring, this technology provides convenient analysis by melting temperatures. PCR products ca
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Mutation Detection by Fluorescent Hybridization Probe Melting Curvesrd for initially characterizing a new region of DNA, it is not a practical solution for the routine analysis of a sequence once it is known. For this reason, molecular techniques that facilitate the analysis of variants in established sequence have widespread application and continue to be developed
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