000			06004nam a2200397 i 4500
999			_c393111 _d393111 _x1
001			393111
003			ES-MaUEC
005			20240314174325.0
006			a|||| o|||| 00| 0
007			cr nn 008mamaa
008			100301s1999 xxu| o |||| 0|eng d
020			_a9781592595846
024	7		_a10.1385/1592595847 _2doi
040			_aES-MaUEC _bspa _cES-MaUEC _dES-MaUEC
050		4	_aQP551 _b1999 EB
245	0	0	_a2-D Proteome Analysis Protocols _cedited by Andrew J. Link
250			_a1st edition 1999
264		1	_aTotowa, NJ _bHumana Press _c1999
300			_a1 recurso en línea (XVII, 601 páginas)
336			_atexto _btxt _2rdacontent
337			_aelectrónico _bc _2rdamedia
338			_arecurso electrónico _bcr _2rdacarrier
347			_aarchivo de texto _bPDF
490	0		_aMethods in Molecular Biology _x1940-6029 _v112
505	0		_a2-D Protein Gel Electrophoresis -- Solubilization of Proteins in 2-D Electrophoresis -- Preparation of Escherichia coli Samples for 2-D Gel Analysis -- Preparing 2-D Protein Extracts from Yeast -- 2-D Protein Extracts from Drosophila melanogaster -- Preparing 2-D Protein Extracts from Caenorhabditis elegans -- Eukaryotic Cell Labeling and Preparation for 2-D -- Differential Detergent Fractionation of Eukaryotic Cells -- Fractionated Extraction of Total Tissue Proteins from Mouse and Human for 2-D Electrophoresis -- Preparation and Solubilization of Body Fluids for 2-D -- 2-D Electrophoresis of Plant Proteins -- Quantifying Protein in 2-D PAGE Solubilization Buffers -- Measuring the Radioactivity of 2-D Protein Extracts -- Advantages and Disadvantages of Carrier Ampholyte IEF -- 2-D Electrophoresis Using Carrier Ampholytes in the First Dimension (IEF) -- Nonequilibrium pH Gel Electrophoresis (NEPHGE) -- High-Resolution, 2-D Protein Electrophoresis Using Nondedicated Equipment -- Large-Gel 2-D Electrophoresis -- Advantages of Immobilized pH Gradients -- Casting Immobilized pH Gradients (IPGs) -- Analytical IPG-Dalt -- IPG-Dalt of Very Alkaline Proteins -- Running Preparative Carrier Ampholyte and Immobilized pH Gradient IEF Gels for 2-D -- In-Gel Sample Rehydration of Immobilized pH Gradient -- High-Resolution, IPG-Based, Mini Two-Dimensional Gel Electrophoresis -- Horizontal SDS-PAGE for IPG-Dalt -- Casting and Running Vertical Slab-Gel Electrophoresis for 2D-PAGE -- Nonreducing 2-D Polyacrylamide Gel Electrophoresis -- 2-D Diagonal Gel Electrophoresis -- 2-D Phosphopeptide Mapping -- Internal Standards for 2-D -- Autoradiography of 2-D Gels -- Double-Label Analysis -- Silver Staining of 2-D Electrophoresis Gels -- Staining of Preparative 2-D Gels -- Electroblotting of Proteins from 2-D Polyacrylamide Gels -- Detection of Total Proteins on Western Blots of 2-D Polyacrylamide Gels -- Protein Detection Using Reversible Metal Chelate Stains -- Glycoprotein Detection of 2-D Separated Proteins -- Image Acquisition in 2-D Electrophoresis -- Computer Analysis of 2-D Images -- 2-D Databases on the World Wide Web -- Comparing 2-D Electrophoretic Gels Across Internet Databases -- Constructing a 2-D Database for the World Wide Web -- Absolute Quantitation of 2-D Protein Spots -- Generating a Bacterial Genome Inventory -- Immunoaffinity Identification of 2-DE Separated Proteins -- 2-DE Spot Amino Acid Analysis with 9-Fluorenylmethyl Chloroformate -- N-Terminal Amino Acid Sequencing of 2-DE Spots -- Characterizing Proteins from 2-DE Gels by Internal Sequence Analysis of Peptide Fragments -- Obtaining Molecular Weights of Proteins and Their Cleavage Products by Directly Combining Gel Electrophoresis with Mass Spectrometry -- Identification of Proteins by Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry Using Peptide and Fragment Ion Masses -- Sample Preparation Methods for Mass Spectrometric Peptide Mapping Directly from 2-DE Gels -- Protein Identification and Analysis Tools in the ExPASy Server -- Automated Protein Identification Using Microcolumn Liquid Chromatography-Tandem Mass Spectrometry -- Peptide Sequencing of 2-DE Gel-Isolated Proteins by Nanoelectrospray Tandem Mass Spectrometry.
520			_aIn 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.
988			_aSpringer_Protocols_1999
650		7	_2embne _9430647 _aProteómica
776	0	8	_iPrinted edition: _z9781617370601
776	0	8	_iPrinted edition: _z9781489943224
776	0	8	_iPrinted edition: _z9780896035249
856	4	0	_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://doi.org/10.1385/1592595847 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
942			_2lcc _cLE
998			_b01/2024 _dz _eb _zSI