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2-D Proteome Analysis Protocols (Methods in Molecular Biology)
 
 
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2-D Proteome Analysis Protocols (Methods in Molecular Biology) [Hardcover]

Andrew J. Link (Editor)

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Book Description

0896035247 978-0896035249 January 15, 1999 1st
A step-by-step tour through the complete process of doing proteomics. With easy-to-follow instructions, complete with many helpful hints and explanations, leading investigators and pioneers in the field show how to make protein extracts, reproducibly run them on 2-D gels, detect them, analyze the data, and precisely identify each protein. The book covers the latest methods of using carrier ampholytes in the 1st dimension, casting and running immobilized pH gradient 2-D gels, MALDI-TOF-based peptide mapping, automated tandem mass spectrometry, and nanoelectrospray ionization technology. For the 2nd dimension, there are methods for running flatbed or vertical gels and for protein detection using autoradiography, and Coomassie, silver, and reversible metal-chelate stains. 2-D Proteome Analysis Protocols is the most complete guide for using proteomics to answer biological questions.

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Editorial Reviews

Review

"Our readers will find in this book with its 55 chapters, written by 78 highly well-trained specialists, all they need to come to a good result, going out from the theory of the subject to the precise description of the protocols, the instrumentation, to additive notes, the problems and the eventual difficulties. In one word, an excellent and practical book."-Cellular and Molecular Biology "...There are 55 chapters covering everything you really need to know to get you to speed in the analysis of the proteome. I really liked the layout of each chapter with a pithy introduction followed by materials and methods sections...an absolute must for the proteomic laboratory."-Microbiology Today ". . .the book covers practical aspects , is well documented, and clearly written . . . recommended for researchers in the field. This collection of protocols is an invaluable starting point for people embarking on attempts to develop new proteomes."-FEBS Letters "The wealth of techniques and helpful hints presented in this book should be useful to both neophytes and advanced researchers engaged in the area of high resolution 2-D protein electrophoresis."-Analytical Biochemistry

From the Back Cover

In 2-D Gel Proteome Analysis Protocols, Andrew Link and his expert collaborators take today's researchers step-by-step through the complete process of doing proteomics. With easy-to-follow instructions, complete with many helpful hints and explanations, leading investigators and pioneers in the field show how to make protein extracts, reproducibly run them on a 2-D gels, detect them, analyze the data, and precisely identify each protein. The book covers the latest methods of using carrier ampholytes in the 1st dimension, casting and running immobilized pH gradient 2-D gels, MALDI-TOF-based peptide mapping, automated tandem mass spectrometry, and nanoelectrospray ionization technology. For the 2nd dimension, there are methods for running flatbed or vertical gels and for protein detection using autoradiography, and Coomassie, silver, and reversible metal-chelate stains. The book is a perfect complement to the genome sequencing project for answering biological questions. 2-D Gel Proteome Analysis Protocols is the most complete guide for using proteomics to answer biological questions. Whether it is a question of global protein analysis or evaluating a cell's response to internal or external stimuli, the advanced methods described here will enable today's researchers better to understand how cells work and open new possibilities for drug discovery.

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Inside This Book (learn more)
First Sentence:
Two-dimensional electrophoresis (2-D) of proteins used to be an art practiced by a few researchers, and their worldwide meetings could be held in a side room of a medium-sized hotel. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
human heart proteins, immunoaffinity identification, cathodic buffer strip, one last selected, very alkaline proteins, metal chelate stains, polymerization cassette, autolytic peptides, electroblotted proteins, yeast protein patterns, nanoelectrospray needle, electrofocusing chamber, sample solubilization buffer, urea mix, tandem mass spectrum, pellet factor, stacker gel, master gel, reswelling cassette, rehydration cassette, match gels, acrylamido buffers, sample rehydration, access related data, selected gels
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Humana Press Inc, Proteome Analysis Protocols Edited, Amersham Pharmacia Biotech, New York, Methods Enzymol, World Wide Web, Argon Dry, San Diego, Rapid Commun, Ogorzalek Loo, Molecular Dynamics, Nondedicated Equipment, San Francisco, Cold Spring Harbor, Rank Score Protein, Spot Amino Acid Analysis, Applied Biosystems, Boehringer Mannheim, Choose Analyze, Components Mixture Final, Detection of Total Proteins, Instaview Nitrocellulose, Netscape Navigator, Nucleic Acids Res, Practical Approach
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