Àâòîðèçàöèÿ
Ïîèñê ïî óêàçàòåëÿì
Gooding K.M., Regnier F.E. — HPLC of biological macromolecules
Îáñóäèòå êíèãó íà íàó÷íîì ôîðóìå
Íàøëè îïå÷àòêó? Âûäåëèòå åå ìûøêîé è íàæìèòå Ctrl+Enter
Íàçâàíèå: HPLC of biological macromolecules
Àâòîðû: Gooding K.M., Regnier F.E.
Àííîòàöèÿ: Completely revised and expanded to reflect the most recent innovations in HPLC from the past decade, this authoritative reference presents practical strategies for the evaluation and analysis of proteins, peptides, and polynucleotides and offers class-specific applications for the characterization and fractionation of biological macromolecules. Contains updated material on organic supports, size exclusion, ion exchange, hydrophobic interaction, and metal interaction chromatography! With contributions from leading experts in the field, the Second Edition of HPLC of Biological Macromolecules provides ·new chapters summarizing specialized detection systems ·current discussions on the chemical and biological properties of specific biomolecules ·detailed guidelines for the development of modern analytical techniques ·state-of-the-art exploration methods for complex mixtures ·successful implementation and investigation procedures With more than 2200 contemporary references—over 1000 more than the previous edition— HPLC of Biological Macromolecules, Second Edition is an essential source for biochemists and analytical biochemists, molecular and cell biologists, biophysicists, geneticists, chemical and biotechnological engineers, biochemical neuroendocrinologists, and upper-level undergraduate and graduate students in these disciplines.
ßçûê:
Ðóáðèêà: Áèîëîãèÿ /
Ñòàòóñ ïðåäìåòíîãî óêàçàòåëÿ: Ãîòîâ óêàçàòåëü ñ íîìåðàìè ñòðàíèö
ed2k: ed2k stats
Èçäàíèå: 2nd edition, revized and expanded
Ãîä èçäàíèÿ: 2002
Êîëè÷åñòâî ñòðàíèö: 777
Äîáàâëåíà â êàòàëîã: 29.11.2005
Îïåðàöèè: Ïîëîæèòü íà ïîëêó |
Ñêîïèðîâàòü ññûëêó äëÿ ôîðóìà | Ñêîïèðîâàòü ID
Ïðåäìåòíûé óêàçàòåëü
Adsorption, isotherms 295—296
Affinity chromatography, antibodies 622—630 655—659
Affinity chromatography, biomimctic ligand 626—627
Affinity chromatography, ligands 334—336
Affinity chromatography, media 33—38 318 322—339
Affinity chromatography, membrane proteins 528—532
Affinity chromatography, protein A 622—625
Affinity chromatography, protein G 624—626
Affinity tags 249—250
Antibodies 607—613
Antibodies, immunodetection 653—659
Biological activity, preservation 285—289
Biological activity, protease inhibitors 286
Capacity factor (k'), effect of displacing species 137—144
Cooperativity 88—89
Data analysis, cereal proteins 562—566
Detergents 177—180 516—519
Detergents in MIC 270
Detergents, membrane proteins 385
Detergents, removal 387—389
Detergents, solubilization 384—387
Diffusion coefficient 63—64
Fermentation, strategies 289—291
Gel filtration chromatography See Size exclusion chromatography
Glycoproteins 635—636
Gradient elution, computer simulation 426—430
Gradient elution, conformational effects 411—414
Gradient elution, molecular weight effect 410—411
Gradient elution, principles 398—410
Gradient elution, systematic development 414—426
Hemoglobin, 599—600
Hemoglobin, , analyzers 601—602
Hemoglobin, , cation-exchange 600—602
Hemoglobin, , immunochemical methods 603
Hemoglobin, , reference methods 602
Hemoglobin, variants 589—591
Hemoglobin, variants, cation-exchange 592—598
Hemoglobin, variants, isoelectric focusing 592
Hemoglobin, variants, reversed-phase 593—599
Hydrodynamic volume 51—56
Hydrophilic interaction chromatography (HILIC), peptides 461—473
Hydrophobic interaction chromatography (HIC) 99—245
Hydrophobic interaction chromatography (HIC), antibodies 620—622
Hydrophobic interaction chromatography (HIC), applications 213—224
Hydrophobic interaction chromatography (HIC), comparison with RPC 116—117 201—202
Hydrophobic interaction chromatography (HIC), glycoproteins 643—646
Hydrophobic interaction chromatography (HIC), historical 103—110
Hydrophobic interaction chromatography (HIC), k' 137—144
Hydrophobic interaction chromatography (HIC), mechanism 125—129
Hydrophobic interaction chromatography (HIC), mobile phase 177—180
Hydrophobic interaction chromatography (HIC), mobile phase effects 129—137
Hydrophobic interaction chromatography (HIC), operation 207—209
Hydrophobic interaction chromatography (HIC), preparative 305 318—321
Hydrophobic interaction chromatography (HIC), sorbents 114—116 156—162
Hydrophobic interaction chromatography (HIC), strategy 197—201
Hydrophobic interaction chromatography (HIC), surface chemistry 163—168
Hydrophobic interactions, mechanisms 125—129 146—156
Hydrophobic interactions, models, preferential interaction 151—152
Hydrophobic interactions, models, solvophobic 146—151
Hydrophobic interactions, models, stoichiometric solvent displacement 152—155
Hydrophobic interactions, surface tension 146—151 177—180
Hydrophobic interactions, temperature, effects of 180—197 200—201
Hydrophobic interactions, thermodynamics 144—146 180—197
Hydroxyapatite chromatography (HAC), antibodies 619—620
Hydroxyapatite chromatography (HAC), glycoproteins 639—641
Immunodetection 653—688
Immunodetection, capillary electrophoretic 666—673
Immunodetection, enhancing sensitivity 673—682
Immunodetection, tandem chromatography 661—666
Ion-exchange chromatography (IEC) 81—98
Ion-exchange chromatography (IEC), antibodies 615—619
Ion-exchange chromatography (IEC), capacity 97—98
Ion-exchange chromatography (IEC), cereal proteins 553—556
Ion-exchange chromatography (IEC), cleaning columns 500
Ion-exchange chromatography (IEC), glycoproteins 638—639
Ion-exchange chromatography (IEC), hemoglobin 592—593
Ion-exchange chromatography (IEC), macromolecules, of 88—91
Ion-exchange chromatography (IEC), membrane proteins 521 525—527 536—537
Ion-exchange chromatography (IEC), mobile phase 95—97
Ion-exchange chromatography (IEC), peptides 452—461
Ion-exchange chromatography (IEC), preparative 303—317
Ion-exchange chromatography (IEC), resins 32—34
Ion-exchange chromatography (IEC), resolution 94—98
Ion-exchange chromatography (IEC), retention 91—94
Ion-exchange chromatography (IEC), sorbents 82—85
Loadability 2
Mass spectrometry (MS), electrospray ionization 693—697
Mass spectrometry (MS), fragmentation 704—709
Mass spectrometry (MS), glycoproteins 646—651
Mass spectrometry (MS), matrix-assisted laser desorption/ionization (MALDI) 697—704
Mass spectrometry (MS), methods 689—704
Mass spectrometry (MS), oligonucleotides 729—734
Mass spectrometry (MS), peptides 720—722
Mass spectrometry (MS), proteins after gel electrophoresis 722—729
Mass spectrometry (MS), recombinant proteins 711—720
Metal interaction chromatography (MIC) 247—280
Metal interaction chromatography (MIC), affinity tags 249—250
Metal interaction chromatography (MIC), amino acid specificity 249—252
Metal interaction chromatography (MIC), antibodies 627—628
Metal interaction chromatography (MIC), applications 272—276
Metal interaction chromatography (MIC), chelating ligates 254—257
Metal interaction chromatography (MIC), glycosylation, effect of 252
Metal interaction chromatography (MIC), metal ions 258—263
Metal interaction chromatography (MIC), mobile phase 263—271
Metal interaction chromatography (MIC), mobile phase, competitive displacers 269—270
Metal interaction chromatography (MIC), mobile phase, detergents 270
Metal interaction chromatography (MIC), mobile phase, organic solvents 270—271
Metal interaction chromatography (MIC), mobile phase, pH 267—269
Metal interaction chromatography (MIC), mobile phase, salt 263—267
Metal interaction chromatography (MIC), multimodal chromatography 276—277
Metal interaction chromatography (MIC), operation 271—272
Metal interaction chromatography (MIC), phosphate specificity 253
Metal interaction chromatography (MIC), stationary phase 253—263
Metal interaction chromatography (MIC), stationary phase, spacer arm 257
Metal interaction chromatography (MIC), stationary phase, support matrix 258
Mixed modality sorbents, hydrophobic 168—170
Mixed modality sorbents, metal ion interaction 276—277
Monolithic columns 11 43—45
Multistep HPLC 440—441
Oligonucleotidcs, MS of 729—734
p1 86—88
Peptide standards 441—442
Peptide standards, conformation 447—448
Peptide standards, IEC 454—461
Peptide standards, RPC 478—490
Peptide standards, SEC 445—446
Peptides 433—511
Peptides, characteristics 434—435
Peptides, column selection 437—441
Peptides, conformation 487—490
Peptides, detection 435—437
Peptides, HILIC/CEC 461—473
Peptides, IEC 452—461
Peptides, MS of 720—722
Peptides, prediction of retention 486—487
Peptides, RPC 473—500
Peptides, SEC 442—451
Peptides, troubleshooting 500—503
Photodiode array (PDA), conformational studies 755—767
Photodiode array (PDA), detector design 741—751
Photodiode array (PDA), flow cell design 745—751
Photodiode array (PDA), wavelength 752—755
Polymer support, agarose 21—22
Polymer support, cellulose 20—21
Polymer support, compressed gels 42
Polymer support, macroporous 22—25
Polymer support, membrane 40—42
Polymer support, monodisperse 38—39
Polymer support, monolith 43—45
Polymer support, pores 19—20 24
Polymer support, preparation 18—19
Polymer support, surface modification 26—27
Polymer support, surface modification, affinity 33—38
Polymer support, surface modification, hydrophobic 31—32
Polymer support, surface modification, ion-exchange 32—34
Polynucleotide, characteristics 282—285
Precipitation 377—378 389—390
Preparative chromatography 281—373
Preparative chromatography, adsorption isotherms 295—296
Preparative chromatography, analytical vs. 294—300
Preparative chromatography, cereal proteins 574
Preparative chromatography, continuous 359—369
Preparative chromatography, continuous, affinity belt 367—369
Preparative chromatography, continuous, affinity recycle extraction 366—367
Preparative chromatography, continuous, annular 363—365
Preparative chromatography, continuous, counter current 369
Preparative chromatography, continuous, membrane 365—366
Preparative chromatography, continuous, simulated moving bed 361—363
Preparative chromatography, equipment 298—300
Preparative chromatography, media 300—351
Preparative chromatography, media, adsorption 341 351
Preparative chromatography, media, affinity 318 322—339
Preparative chromatography, media, hydrophobic interaction 305 318—321
Preparative chromatography, media, ion-exchange 303—317
Preparative chromatography, media, modes 301—304
Preparative chromatography, media, particle size 352—353
Preparative chromatography, media, reversed phase 341 349—350
Preparative chromatography, media, size exclusion 336 342—348
Preparative chromatography, media, sorbents 301—302
Preparative chromatography, modes 296—298
Preparative chromatography, packing columns 357—359
Preparative chromatography, productivity 353—356
Preparative chromatography, scale-up 356—359
Pressure 183
Pressure in preparative chromatography 300—301
Protease inhibitors 286
Protein structure, characteristics 117—118 281—282
Protein structure, conformation by PDA 755—767
Protein structure, folding 191—197
Protein structure, solvent effects 118—120
Protein structure, spectroscopic elucidation 120—124 202—207
Protein structure, thermodynamics 180—197
Proteins, cereal 547—548
Proteins, cereal, characterization 566—570
Proteins, cereal, genetic studies 573—574
Proteins, cereal, quality 576—578
Proteins, cereal, varietal identification 570—573
Proteins, fusion 336 340
Proteins, membrane 513—516
Proteins, membrane, troubleshooting 532—535
Proteins, recombinant by MS 711—720
Proteins, therapeutic 292—294
Retention, models 146—155
Reversed-phase chromatography (RPC) 99—245
Reversed-phase chromatography (RPC), applications 209—212 222—224
Reversed-phase chromatography (RPC), cereal proteins 551—557
Reversed-phase chromatography (RPC), cleaning columns 501—502
Reversed-phase chromatography (RPC), comparison with HIC 116—117 201—202
Reversed-phase chromatography (RPC), glycoproteins 641—644
Reversed-phase chromatography (RPC), historical 103—110
Reversed-phase chromatography (RPC), ion pair agents 473—478 490—491
Reversed-phase chromatography (RPC), k' 137—144
Reversed-phase chromatography (RPC), mechanism 125—129
Reversed-phase chromatography (RPC), membrane proteins 530—534 537—540
Reversed-phase chromatography (RPC), mobile phase, effects 129—137
Reversed-phase chromatography (RPC), mobile phase, general 170—173
Reversed-phase chromatography (RPC), mobile phase, organic solvent 173—177
Reversed-phase chromatography (RPC), mobile phase, salts 177—180
Reversed-phase chromatography (RPC), operation 207—209
Reversed-phase chromatography (RPC), peptides 473—500
Reversed-phase chromatography (RPC), preparative 341 349—350
Reversed-phase chromatography (RPC), sorbents 110—114 156—162
Reversed-phase chromatography (RPC), strategy 197—201
Reversed-phase chromatography (RPC), surface chemistry 162—163
Sample preparation 375—395
Sample preparation, antibodies 613—614
Sample preparation, cereal proteins 548—551 560—561
Sample preparation, concentration 389—390
Sample preparation, desalting 391—392
Sample preparation, detergent removal 387—389
Sample preparation, extraction, liquid-liquid 378
Sample preparation, extraction, liquid-solid 378
Sample preparation, extraction, solid-phase (SPE) 379—384
Sample preparation, extraction, supercritical flow 378
Sample preparation, membrane proteins 519
Sample preparation, solubilization 384—387
Sample preparation, ultrafiltration 390
Silica, 6—7
Silica, calcination 5
Silica, pores 3—4 9
Silica, preparation 11—12
Silica, stability 10
Silica, structure 3
Silica, surface 4—7
Silica, surface area 9
Size exclusion chromatography (SEC) 49—79
Size exclusion chromatography (SEC), 50—52
Size exclusion chromatography (SEC), antibodies 614—616
Size exclusion chromatography (SEC), band spreading 61—64
Size exclusion chromatography (SEC), cereal proteins 552—554 556
Size exclusion chromatography (SEC), cleaning columns 500
Size exclusion chromatography (SEC), loading capacity 72
Size exclusion chromatography (SEC), membrane proteins 521—524 535—536
Size exclusion chromatography (SEC), methodology 69—72
Size exclusion chromatography (SEC), mobile phase 69—70
Size exclusion chromatography (SEC), nonideal 72—75 443—445
Size exclusion chromatography (SEC), peptides 442—451
Size exclusion chromatography (SEC), preparative 336 342—348
Size exclusion chromatography (SEC), resolution 56—64
Size exclusion chromatography (SEC), supports 64—68
Size exclusion chromatography (SEC), troubleshooting 77
Solid-phase extraction (SPE) 379—384
Solid-phase extraction (SPE), batch 379
Solid-phase extraction (SPE), cartridge 380—384
Solubilization 384—387
Spectroscopy, protein conformation 120—124 202—207
Surface tension 146—151
Temperature, effect of, cereal proteins 557—559
Temperature, effect of, hydrophobic interactions 180—197 200—201
Temperature, effect of, peptides 495—497
Titration curves 86—88
Void volume 50—51
Ðåêëàìà