2-D Proteome Analysis Protocols (Methods in Molecular Biology, 112) Hardback - 1998
by Link, Andrew J
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Details
- Title 2-D Proteome Analysis Protocols (Methods in Molecular Biology, 112)
- Author Link, Andrew J
- Binding Hardback
- Edition 1999
- Condition Used: Good
- Pages 601
- Volumes 1
- Language ENG
- Publisher Humana, Totowa, New Jersey, U.S.A
- Publication date 1998-09-24
- Illustrated Yes
- Features Bibliography, Illustrated, Index, Table of Contents
- Bookseller's Inventory # SONG0896035247
- ISBN 9780896035249 / 0896035247
- Weight 2.38 lbs (1.08 kg)
- Dimensions 9 x 6 x 1.5 in (22.86 x 15.24 x 3.81 cm)
- Size 6.00x1.50x9.00
- Category Science
- Library of Congress subjects Proteins - Analysis, Gel electrophoresis
- Library of Congress Catalogue Number 98038677
- Dewey Decimal Code 572.6
- Quantity available 1
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From the publisher
From the rear 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.