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Titlebook: Chromatin Protocols; Peter B. Becker Book 19991st edition Springer Science+Business Media New York 1999

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書(shū)目名稱Chromatin Protocols
編輯Peter B. Becker
視頻videohttp://file.papertrans.cn/227/226299/226299.mp4
叢書(shū)名稱Methods in Molecular Biology
圖書(shū)封面Titlebook: Chromatin Protocols;  Peter B. Becker Book 19991st edition Springer Science+Business Media New York 1999
描述More than 40 years after the discovery of the nucleosome as the fun- mental unit of chromatin, the multifaceted problem of how variations in ch- matin structure affect the activity of the eukaryotic genome has not been solved. However, during the past few years research on chromatin structure and fu- tion has gained considerable momentum, and impressive progress has been made at the level of concept development as well as filling in crucial detail. The structure of the nucleosome has been visualized at unprecedented reso- tion. Powerful multisubunit enzymes have been identified that alter histone/ DNA interactions in ways that expose regulatory sequences to factors initi- ing and regulating such nuclear processes as transcription. Though the imp- tance of posttranslational modifications of histones, notably their acetylation, has long been known, the finding that a number of bona fide regulators increase transcription by acetylating nucleosomes has lent new support to the old idea that the process of gene regulation is intimately related to the nature of the chromatin environment. A wealth of nonhistone proteins contribute to a continuum of structures with distinct biochemical prop
出版日期Book 19991st edition
版次1
doihttps://doi.org/10.1385/1592596819
isbn_ebook978-1-59259-681-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 1999
The information of publication is updating

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Springer Tracts in Modern Physicsnot be viewed by these methods. This problem was overcome by extraction of histone from chromosomes, followed by microscopic visualization of the residual structures (.–.). This led to the suggestion that chromatin fibers were organized into domains, loops attached to a proteinaceous framework calle
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Mathematical Details and Additional Physics, can be reproduced in crude extracts derived from Xenopus oocytes or eggs (.–.), . embryos (.–.), or from human cells (.–.). Extracts competent for the NER process can be derived from a variety of cultured mammalian cells (.,.), cultured . cells (.), and . eggs (.).
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Springer Tracts in Modern Physicsro reconstituted chromatin. SV40 MCs are especially useful in approaching questions regarding stages in transcriptional activation from a potentially competent to a fully active state. Furthermore, because of the utility of SV40 as a viral vector for exogenous promoters (.,.), fully functional cellu
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Expression and Purification of Recombinant Histones and Nucleosome Reconstitution,ons of histone proteins give rise to heterogeneity. The extent of heterogeneity and modification strongly depend on the type and developmental state of the tissue from which chromatin is isolated and can vary significantly between different batches. Fourth, and most important, only naturally occurri
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Base-Pair Resolution Mapping of Nucleosomes In Vitro, histone proteins. The more rigorous fixing of the exact region of DNA in contact with the histone octamer is known as translational positioning. This not only implies a rotational phase, but also locates the detailed features of nucleosomal DNA relative to the histone octamer structure for a partic
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