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portada dna topoisomerase protocols: volume i: dna topology and enzymes
Type
Physical Book
Publisher
Year
2010
Language
English
Pages
327
Format
Paperback
Dimensions
22.9 x 15.2 x 2.0 cm
Weight
0.50 kg.
ISBN
1617370398
ISBN13
9781617370397

dna topoisomerase protocols: volume i: dna topology and enzymes

Neil Osheroff (Illustrated by) · Mary-Ann Bjornsti (Illustrated by) · Humana · Paperback

dna topoisomerase protocols: volume i: dna topology and enzymes - Bjornsti, Mary-Ann ; Osheroff, Neil

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£ 118.63

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Synopsis "dna topoisomerase protocols: volume i: dna topology and enzymes"

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 chapters are written by prominent investigators in the field and provide detailed background information and st- by-step experimental protocols. The topics covered in Volume I; DNA Topology and Enzymes, range from detailed methods to analyze various aspects of DNA structure, from linking number, knotting/unknotting, site-specific recombi- tion, and decatenation to the overexpression and purification of bacterial and eukaryotic DNA topoisomerases from a variety of cell systems and tissues.

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