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Gooding K.M., Regnier F.E. — HPLC of biological macromolecules
Gooding K.M., Regnier F.E. — HPLC of biological macromolecules



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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: en

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
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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, $A_{1c}$      599—600
Hemoglobin, $A_{1c}$, analyzers      601—602
Hemoglobin, $A_{1c}$, cation-exchange      600—602
Hemoglobin, $A_{1c}$, immunochemical methods      603
Hemoglobin, $A_{1c}$, 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, $pK_a$      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), $K_D$      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
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