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Titlebook: Differential Display Methods and Protocols; Peng Liang,Arthur B. Pardee Book 19971st edition Humana Press 1997

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书目名称Differential Display Methods and Protocols
编辑Peng Liang,Arthur B. Pardee
视频video
丛书名称Methods in Molecular Biology
图书封面Titlebook: Differential Display Methods and Protocols;  Peng Liang,Arthur B. Pardee Book 19971st edition Humana Press 1997
描述Of the estimated 80,000 individual genes encoded by the human genome, approximately 10-20% are expressed by the average cell. This subset is a major determinant of a cell‘s properties. In addition to the control of cellular phenotype and the normal physiological processes of an organism, an alt- ation in gene expression (either induction or repression) underlies the etiology of numerous, diverse pathological processes. Therefore understanding the mechanisms of these normal and pathological processes requires identifi- tion, isolation, and characterization of differentially expressed genes. This requirement has led to the development of a variety of techniques capable of identifying small quantities of proteins or mRNAs that are key to a multitude of diverse pathological processes. Differential display (DD) is an emerging "fingerprinting" technology that facilitates the identification of mRNAs in a cell or tissue, in particular those with altered expression resulting from diff- ences in transcription or mRNA degradation. In contrast to conventional te- niques, DD can be used to compare mRNA expressions in many samples created under multiple experimental conditions. DD was conceived
出版日期Book 19971st edition
版次1
doihttps://doi.org/10.1385/0896034895
isbn_ebook978-1-59259-569-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 1997
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Differential Display Using Random Hexamer-Primed cDNA, Motif Primers, and Agarose Gel Electrophoresintracellular signal transduction pathways. One cellular response to mitogenic stimulation is the sequential transcriptional induction of specific nuclear genes encoding proteins of diverse functions (reviewed in refs. . and .). Many of these proteins are likely to be required for DNA replication and
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Differential Screening of Differential Display cDNA Products by Reverse Northernen made to improve and optimize the technique (.,.). One major bottle-neck remains, though, in the screening step for the verification of the cDNA fragments tentatively identified by differential display.
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Cloning of the 3′ Noncoding Regions from Several Members of Heat Shock Protein Gene Families by Diff of a gene family, it is essential to isolate the representative cDNAs encoding the protein of interest. In the past, this has been especially difficult owing to highly similar protein coding region of the cDNAs from a gene family with minute variations in their amino acid composition. The 3′ noncod
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