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Protein-DNA Interactions, Volume 208: Volume 208: Protein - Dna Interactions (Methods in Enzymology)
 
 
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Protein-DNA Interactions, Volume 208: Volume 208: Protein - Dna Interactions (Methods in Enzymology) [Hardcover]

John N. Abelson (Editor), Melvin I. Simon (Editor), Robert T. Sauer (Editor)

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Book Description

December 25, 1991 0121821099 978-0121821098 1
Methods widely used in the study of DNA binding proteins are presented in this volume. These include purification and protein characterization, assays of protein-DNA binding and protein-induced bending, and biochemical and genetic methods for probing the structure, energy, and specificity of protein-DNA interactions.

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Editorial Reviews

Review

Praise for the Series
"The Methods in Enzymology series represents the gold-standard."
--NEUROSCIENCE
"Incomparably useful."
--ANALYTICAL BIOCHEMISTRY
"It is a true 'methods' series, including almost every detail from basic theory to sources of equipment and reagents, with timely documentation provided on each page."
--BIO/TECHNOLOGY
"The series has been following the growing, changing and creation of new areas of science. It should be on the shelves of all libraries in the world as a whole collection."
--CHEMISTRY IN INDUSTRY
"The appearance of another volume in that excellent series, Methods in Enzymology, is always a cause for appreciation for those who wish to successfully carry out a particular technique or prepare an enzyme or metabolic intermediate without the tiresome prospect of searching through unfamiliar literature and perhaps selecting an unproven method which is not easily reproduced."
--AMERICAN SOCIETY OF MICROBIOLOGY NEWS
"If we had some way to find the work most often consulted in the laboratory, it could well be the multi-volume series Methods in Enzymology...a great work."
--ENZYMOLOGIA
"A series that has established itself as a definitive reference for biochemists."
--JOURNAL OF CHROMATOGRAPHY

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Inside This Book (learn more)
First Sentence:
One of the important early steps in purifying a DNA-binding protein is to separate the protein of interest from cellular nucleic acids. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
consensus base pair, rapid equilibrium limit, average binding density, permanganate pattern, amino acid under study, cleavage loci, nucleoside technique, binding density function, missing nucleoside experiment, hydroxyl radical cleavage reaction, streptomycin selection, diminished cleavages, extension probing, lactose repressor protein, mobility shift gel, reporter promoter, binding and bending, hydroxyl radical footprints, tract bend, arc gene, favorable contacts, nucleosome reconstitution, substituted protein, cro protein, affinity cleaving
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Nucleic Acids Res, New York, Cold Spring Harbor, Academic Press, Genes Deu, Experimental Methods, Laboratory Manual, Molecular Cloning, National Institutes of Health, Practical Approach, San Francisco, Trends Biochem, Case Three, Complex Exists, Molecular Genetics, New England Biolabs, Reagent Protein, San Diego, United States Biochemical, University of Wisconsin-Madison
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