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Titlebook: DNA Topoisomerase Protocols; Volume I: DNA Topolo Mary-Ann Bjornsti,Neil Osheroff Book 1999 Humana Press 1999

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书目名称DNA Topoisomerase Protocols
副标题Volume I: DNA Topolo
编辑Mary-Ann Bjornsti,Neil Osheroff
视频video
丛书名称Methods in Molecular Biology
图书封面Titlebook: DNA Topoisomerase Protocols; Volume I: DNA Topolo Mary-Ann Bjornsti,Neil Osheroff Book 1999 Humana Press 1999
描述Beginning with the Escherichia coli co protein, or bacterial DNA topoisomerase I, an ever-increasing number of enzymes has been identified that catalyze changes in the linkage of DNA strands. DNA topoisomerases are ubiquitous in nature and have been shown to play critical roles in most p- cesses involving DNA, including DNA replication, transcription, and rec- bination. These enzymes further constitute the cellular targets of a number of clinically important antibacterial and anticancer agents. Thus, further studies of DNA topology and DNA topoisomerases are critical to advance our und- standing of the basic biological processes required for cell cycle progression, cell division, genomic stability, and development. In addition, these studies will continue to provide critical insights into the cytofoxic action of drugs that target DNA topoisomerases. Such mechanistic studies have already played an important role in the development and clinical application of antimicrobial and chemotherapeutic agents. The two volumes of DNA Topoisomerase Protocols are designed to help new and established researchers investigate all aspects of DNA topology and the function of these enzymes. The chapte
出版日期Book 1999
版次1
doihttps://doi.org/10.1385/1592592597
isbn_softcover978-1-61737-039-7
isbn_ebook978-1-59259-259-3Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 1999
The information of publication is updating

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Two-Dimensional Agarose-Gel Electrophoresis of DNA Topoisomers,DNA molecules of totally different structures may have the same electrophoretic mobility. These DNA species can be resolved by two-dimensional (2-D) gel electrophoresis, which involves two successive operations carried out with one gel slab under different conditions and in orthogonal directions.
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Purification of Supercoiled Plasmid DNA,he capability of generating both positive and negative DNA supercoils during the process of transcription and replication, respectively. These supercoils must be relaxed in order for transcription and replication to continue unaffected, as outlined in preceding chapters. The DNA topoisomerases play
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Purification and Use of DNA Minicircles with Different Linking Numbers,information in topologically independent domains consisting of one or more genes and of all the elements required in cis for their functioning. The elements that belong to the same functional unit are topologically linked: they depend on each other and cooperate.
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Isolation of Knotted DNA from Coliphage P4,ssay for type II topoisomerase activity, even in crude extracts. Such assays have been useful in screening drugs that are suspected to inhibit type II topoisomerases. This chapter describes the isolation of knotted DNA from P4 phage. In the case of wild-type P4, such DNA molecules are double-strande
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Sedimentation Analysis of Bacterial Nucleoid Structure,f extracted nucleoids. Since the few DNA nicks that occur when nucleoids are isolated (.,.) are localized by the presence of 50–100 barriers to strand rotation (.,.), it is possible to recover chromosomal DNA in which most of each molecule is topologically constrained (.,.). Consequently, intracellu
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