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Titlebook: Generation of cDNA Libraries; Methods and Protocol Shao-Yao Ying Book 2003 Humana Press 2003

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发表于 2025-3-21 16:29:34 | 显示全部楼层 |阅读模式
书目名称Generation of cDNA Libraries
副标题Methods and Protocol
编辑Shao-Yao Ying
视频video
概述Includes supplementary material:
丛书名称Methods in Molecular Biology
图书封面Titlebook: Generation of cDNA Libraries; Methods and Protocol Shao-Yao Ying Book 2003 Humana Press 2003
描述Since its invention and subsequent development nearly 20 years ago, po- merase chain reaction (PCR) has been extensively utilized to identify numerous gene probes in vitro and in vivo. However, attempts to generate complete and full-length complementary cDNA libraries were, for the most part, fruitless and remained elusive until the last decade, when simple and rapid methods were developed. With current decoding and potential application of human genome information to genechips, there are urgent needs for identification of functional significance of these decoded gene sequences. Inherent in bringing these app- cations to fruition is the need to generate a complete and full-length cDNA library for potential functional assays of specific gene sequences. Generation of cDNA Libraries: Methods and Protocols serves as a laboratory manual on the evolution of generation of cDNA libraries, covering both ba- ground information and step-by-step practical laboratory recipes for which p- tocols, reagents, operational tips, instrumentation, and other requirements are detailed. The first chapter of the book is an overview of the basics of generating cDNA libraries, which include the following: (a
出版日期Book 2003
版次1
doihttps://doi.org/10.1385/1592593593
isbn_softcover978-1-61737-333-6
isbn_ebook978-1-59259-359-0Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 2003
The information of publication is updating

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发表于 2025-3-21 23:36:10 | 显示全部楼层
https://doi.org/10.1057/9780230316973protein. The basis of the widely used novel strategies for the generation of cDNA libraries are base pair complementarities, reverse transcription, and polymerase chain reactions. This chapter presents some general information on the principles of, biology behind, basic protocols of, and reagents us
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Definitions and Conversions of Unitsmprehensive analysis is most frequently carried out on a single-clone-for-single-gene basis, whereas gene discovery is done through the isolation of multiple cDNA clones for a single gene. Thus, current requirements for high-quality cDNA libraries suitable for comprehensive cDNA analysis are (1) hig
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https://doi.org/10.1007/978-3-319-93236-1hods. A minimum of several thousand cells is needed for an acceptable quality of RNA extraction. Because of tissue heterogeneity, these methods usually provided neither reliable nor reproducible results. Unfortunately, it is impossible to collect adequate amounts of pure or homogeneous samples for t
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Convex Bodies and Hypersurfaces structure at the 5′ end of eukaryotic mRNA to design novel methods for PCR-based cDNA library construction (.–.). Moreover, the strategy has been applied to identifying gene expression and isolating full-length cDNA (.–.). In our laboratory, the conventional and PCR-based strategies have been utili
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