Activity coefficients in electrolyte solutions / Ricardo M. Pytkowicz |
Autore | Pytkowicz, Ricardo M. |
Pubbl/distr/stampa | Boca Raton : CRC press, 1979 |
Descrizione fisica | 2 v. ; 26 cm |
Disciplina | 541.372 |
Soggetto non controllato |
Chimica fisica
Termodinamica delle soluzioni |
ISBN |
0-8493-5411-0
0-8493-5412-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | 1 v.: Volume I 2 v.: Volume II |
Record Nr. | UNIPARTHENOPE-000008117 |
Pytkowicz, Ricardo M. | ||
Boca Raton : CRC press, 1979 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Parthenope | ||
|
Allozyme electrophoresis : a handbook for animal systematics and population studies / Barry John Richardson |
Autore | Richardson, Barry John |
Pubbl/distr/stampa | San Diego, : Academic Press, 1986 |
Descrizione fisica | XII, 410 p. : ill. ; 23 cm |
Disciplina |
591.19
541.372 |
Soggetto non controllato |
Fisiologia animale
Enzimi |
ISBN | 0-12-587840-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNINA-990001742080403321 |
Richardson, Barry John | ||
San Diego, : Academic Press, 1986 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Application of Ionic Liquids in Biotechnology / / edited by Toshiyuki Itoh, Yoon-Mo Koo |
Edizione | [1st ed. 2019.] |
Pubbl/distr/stampa | Cham : , : Springer International Publishing : , : Imprint : Springer, , 2019 |
Descrizione fisica | 1 online resource (X, 336 p. 167 illus., 25 illus. in color.) |
Disciplina | 541.372 |
Collana | Advances in Biochemical Engineering/Biotechnology |
Soggetto topico |
Solucions iòniques
Biotecnologia Biotechnology Biophysics Biological physics Physical chemistry Green chemistry Biomaterials Biomedical engineering Biological and Medical Physics, Biophysics Physical Chemistry Green Chemistry Biomedical Engineering/Biotechnology |
Soggetto genere / forma | Llibres electrònics |
ISBN | 3-030-23081-3 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Ionic Liquids in Bioseparation Processes -- DES/NADES for Biological Applications -- Ionic Liquid Pretreatment of Lignocellulosic Biomass for Enzymatic Delignification -- Activation of biocatalyst using ionic liquids -- Microbially catalyzed transformation in Ionic Liquids -- ILs for the preparation of biopolymer-based hydrogels -- Advances in processing biomaterials from Ionic liquids -- Synthesis of ionic liquids originated from natural products -- Hydrated ionic liquids as stabilization and refolding media for proteins -- Extraction and isolation of medicinal compounds from bioresources using ionic liquids -- Environmental concerns of ionic liquids in biotechnological applications. |
Record Nr. | UNINA-9910349518403321 |
Cham : , : Springer International Publishing : , : Imprint : Springer, , 2019 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Application of Ionic Liquids on Rare Earth Green Separation and Utilization / / edited by Ji Chen |
Edizione | [1st ed. 2016.] |
Pubbl/distr/stampa | Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 |
Descrizione fisica | 1 online resource (260 p.) |
Disciplina | 541.372 |
Collana | Green Chemistry and Sustainable Technology |
Soggetto topico |
Chemical engineering
Metals Sustainable development Inorganic chemistry Industrial Chemistry/Chemical Engineering Metallic Materials Sustainable Development Inorganic Chemistry |
ISBN | 3-662-47510-3 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Part I Introduction -- Ionic Liquids in the Context of Rare Earth Separation and Utilization -- Part II Chemistry of ionic liquids with rare earth -- Using Crystal Structures of Ionic Compounds to Explore Complexation and Extraction of Rare Earth Elements in Ionic Liquids -- Part III Ionic liquids for the extraction and separation of rare earth -- Separating Rare Earth Elements with Ionic Liquids -- Ionic Liquid-Based Extraction and the Application to Liquid Membrane Separation of Rare Earth Metals -- Application of Ionic Liquids Extractants on Rare Earth Green Separation -- Part IV Electrodeposition of rare earth metal in ionic liquids -- Electrodeposition of Rare Earth Metal in Ionic Liquids -- Part V of Ionic liquids for rare earth utilization -- Ionic Liquids and Rare Earth Soft Luminescent Materials -- Photo functional Rare Earth Materials Based on Ionic Liquids -- Ionic liquid – assisted hydrothermal synthesis of rare earth luminescence materials. |
Record Nr. | UNINA-9910254055003321 |
Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2016 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Biopolymer electrolytes : fundamentals and applications in energy storage / / Y. N. Sudhakar, M. Selvakumar, D. Krishna Bhat |
Autore | Sudhakar Y. N. |
Pubbl/distr/stampa | Amsterdam, Netherlands : , : Elsevier, , [2018] |
Descrizione fisica | 1 online resource (194 pages) |
Disciplina | 541.372 |
Soggetto topico |
Polyelectrolytes
Biopolymers Electrolytes Electrochemistry |
ISBN |
0-12-813611-1
0-12-813447-X |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | An introduction of biopolymer electrolytes -- Methods of preparation of biopolymer electrolytes -- Biopolymer electrolyte for supercapacitor -- Biopolymer electrolytes for solar cells and electrochemical cells -- Biopolymer electrolytes for fuel cell applications -- Biopolymer degradation. |
Record Nr. | UNINA-9910583333603321 |
Sudhakar Y. N. | ||
Amsterdam, Netherlands : , : Elsevier, , [2018] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Capillary electrophoresis : theory & practice / edited by Paul D. Grossman, Joel C. Colburn |
Pubbl/distr/stampa | London, : Academic, 1992 |
Descrizione fisica | xvi, 352 p. ; 24 cm. |
Disciplina |
572.36(Biochimica analitica)
541.372(Soluzioni elettrolitiche) |
ISBN | 01-230-4250-x |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNICAMPANIA-SUN0018822 |
London, : Academic, 1992 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Vanvitelli | ||
|
Capillary electrophoresis : theory & practice / edited by Paul D. Grossman, Joel C. Colburn |
Pubbl/distr/stampa | London, : Academic, 1992 |
Descrizione fisica | xvi, 352 p. ; 24 cm |
Disciplina |
572.36(Biochimica analitica)
541.372(Soluzioni elettrolitiche) |
ISBN | 01-230-4250-x |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNICAMPANIA-VAN0018822 |
London, : Academic, 1992 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Vanvitelli | ||
|
Capillary electrophoresis : theory & practice / edited by Paul D. Grossman, Joel C. Colburn |
Pubbl/distr/stampa | London, : Academic, 1992 |
Descrizione fisica | xvi, 352 p. ; 24 cm |
Disciplina |
572.36(Biochimica analitica)
541.372(Soluzioni elettrolitiche) |
ISBN | 01-230-4250-x |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Record Nr. | UNICAMPANIA-VAN00018822 |
London, : Academic, 1992 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Vanvitelli | ||
|
Capillary electrophoresis -- mass spectrometry for proteomics and metabolomics : principles and applications / / edited by Rawi Ramautar and David D. Y. Chen |
Pubbl/distr/stampa | Hoboken, New Jersey : , : John Wiley & Sons, , [2023] |
Descrizione fisica | 1 online resource (403 pages) |
Disciplina | 541.372 |
Soggetto topico | Capillary electrophoresis |
ISBN |
3-527-83309-9
3-527-83308-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Capillary Electrophoresis-Mass Spectrometry Interfacing: Principles and Recent Developments -- 1.1 Introduction -- 1.2 General Considerations of CE-ESI-MS -- 1.2.1 Electrospray Ionization -- 1.2.2 Electrical Circuit in CE-ESI-MS -- 1.2.3 CE Modes and Conditions in CE-MS -- 1.3 Sheath Liquid Interfaces -- 1.3.1 Coaxial Sheath‐Flow ESI-MS Interface -- 1.3.2 Nanoflow Sheath Liquid ESI-MS Interface -- 1.4 Sheathless Interfaces -- 1.4.1 Porous‐Tip Interface -- 1.4.2 Other Sheathless Interfaces -- 1.5 Other CE-ESI-MS Interfaces -- 1.5.1 Liquid Junction -- 1.5.2 Interface‐Free CE-MS -- 1.6 Microchip Electrophoresis-MS Interfaces -- 1.7 Alternative Ionization Techniques for CE-MS -- 1.7.1 CE and MCE Combined with MALDI-MS -- 1.7.2 CE-ICP-MS -- 1.8 Concluding Remarks and Outlook -- List of Abbreviations -- References -- Chapter 2 Data Analysis Strategies in CE-MS for Metabolomics -- 2.1 Introduction -- 2.2 The Annotation Challenge in CE-MS‐Based Untargeted Metabolomics -- 2.2.1 Peak Picking in CE-MS Metabolomics -- 2.2.2 Alignment Approaches -- 2.2.3 μeff Transformation -- 2.2.3.1 Historical Evolution and Current State -- 2.2.3.2 Quantitative Aspects of the Use of Mobilograms -- 2.2.3.3 Technical Considerations of the μeff Transformation -- 2.2.4 Reproducibility and Exchange of μeff Information Using Libraries -- 2.2.5 Interlaboratory Reproducibility -- 2.2.6 ROMANCE -- 2.2.7 Ion Mobility -- 2.3 Data Pretreatment -- 2.3.1 Area Normalization -- 2.3.2 Analytical Quality Monitoring -- 2.3.3 Data Filtering -- 2.4 Data Treatment -- 2.5 Concluding Remarks -- Acknowledgment -- References -- Chapter 3 Data‐Processing Workflow for Relative Quantification from Label‐Free and Isobaric Labeling‐Based Untargeted Shotgun Proteomics: From Database Search to Differential Expression Analysis.
3.1 Introduction -- 3.2 Spectra Acquisition and Database Search -- 3.2.1 Parameters Affecting Sequence Database Search -- 3.2.1.1 Database Selection -- 3.2.1.2 Enzyme Specificity and Missed Cleavages -- 3.2.1.3 Posttranslational Modifications -- 3.2.1.4 Precursor Mass Tolerance -- 3.2.2 Target-Decoy Search Strategy for False Discovery Rate Estimation -- 3.2.3 Database Search Engines -- 3.2.3.1 SEQUEST -- 3.2.3.2 Mascot -- 3.2.3.3 Multiple Search Engines -- 3.2.4 Protein Inference -- 3.3 Relative Protein Quantification -- 3.3.1 Filtering -- 3.3.2 Missing Value Imputation -- 3.3.2.1 Imputation Methods -- 3.3.2.2 Comparative Studies -- 3.3.2.3 Normalization -- 3.3.3 Summarization -- 3.3.4 Differential Expression Analysis -- 3.4 Conclusions -- References -- Chapter 4 Data Processing in Metabolomics Capillary Electrophoresis-Mass Spectrometry -- 4.1 Data Extraction and the Interpretation of the Extracted Data -- 4.2 Data Preprocessing -- 4.2.1 Handling Missing Values -- 4.2.2 Normalization -- 4.2.3 Transformation -- 4.2.4 Scaling -- 4.3 Statistical Analysis -- 4.3.1 Two‐Sample T‐Test -- 4.3.2 Principal Component Analysis (PCA) -- 4.3.3 Partial Least‐Squares Discriminant Analysis (PLS-DA) -- 4.3.4 Support Vector Machine -- 4.3.5 Logistic Regression -- 4.3.6 Random Forest Model -- 4.3.7 Evaluation of Classification Models -- 4.4 Metabolite Identification -- References -- Chapter 5 Utility and Advances of Capillary Electrophoresis-Mass Spectrometry for Metabolomics -- 5.1 Introduction -- 5.2 Technological Developments -- 5.2.1 Improving Sensitivity -- 5.2.2 Increasing Metabolome Coverage -- 5.2.3 Increasing Annotation Capacity -- 5.2.4 Tackling Anionic Profiling -- 5.2.5 Increasing Sample Throughput -- 5.3 Applications -- 5.3.1 Biomedical Samples -- 5.3.2 Microbial Extracts -- 5.3.3 Plants -- 5.4 Concluding Remarks -- Acknowledgment -- Conflict of Interest. References -- Chapter 6 Comprehensive Lipid Profiling by Multisegment Injection-Nonaqueous Capillary Electrophoresis-Mass Spectrometry: Expanding Coverage Beyond Hydrophilic Metabolites -- 6.1 The Early Origins of Lipidomics -- 6.2 Major Instrumental Platforms in Lipidomics: The Role of Separation Science -- 6.3 NACE-MS: An Emerging Separation Platform for Lipidomics? -- 6.4 Multiplexed Separations for Fatty Acids by MSI-NACE-MS -- 6.5 Comprehensive Lipid Profiling Strategies by MSI-NACE-MS -- 6.6 Future Perspectives and Summary -- References -- Chapter 7 Strategies for Identification of Modified Amino Acids with CE-MS in Metabolomics -- 7.1 Introduction -- 7.1.1 Post‐Translational Modifications and Modified Amino Acids -- 7.1.2 Modified Amino Acids as Biomarkers of Pathologies -- 7.2 Methods for the Detection of Modified Amino Acids -- 7.3 Capillary Electrophoresis Coupled to Mass Spectrometry to Analyze Modified Amino Acids -- 7.3.1 Applications of CE-MS for Analysis of Modified Amino Acids -- 7.4 Recent Developments to Enhance and Facilitate the Annotation Process in CE-MS -- Acknowledgments -- References -- Chapter 8 CE-MS Approaches for Single‐Cell Metabolomics -- 8.1 Introduction -- 8.2 Techniques for Single‐Cell Metabolome Analysis -- 8.2.1 Highly Sensitive CE-MS Interfacing -- 8.2.2 Online Sample Preconcentration Techniques -- 8.2.3 Isolation of Single Cells -- 8.3 Application to Single‐Cell Metabolome Analysis -- 8.3.1 Metabolome Analysis of Large Single Cells with Highly Sensitive Interface -- 8.3.2 Single‐Cell Metabolome Analysis with Highly Sensitive Interface and OSP Method -- 8.3.3 Single‐Cell Metabolome Analysis by Online Sampling and Highly Sensitive Interface -- 8.4 Conclusions -- References -- Chapter 9 CE-MS Approaches for Peptidomics -- 9.1 Introduction -- 9.2 Sample Preparation -- 9.3 CE-MS -- 9.3.1 Basic Characterization. 9.3.2 Peptide Identification -- 9.3.3 Peptide Quantitation -- 9.4 Applications -- 9.4.1 Search, Identification, and Determination of Biomarkers -- 9.4.2 Food Peptidomics -- 9.4.3 Other Applications -- 9.5 Conclusions -- Acknowledgments -- List of Abbreviations -- References -- Chapter 10 Capillary Zone Electrophoresis-Mass Spectrometry for Top‐Down Proteomics: Technological Development and Biological Applications -- 10.1 Introduction -- 10.2 Technological Development -- 10.2.1 CE-MS Interface -- 10.2.2 Capillary Coating -- 10.2.3 Sample Loading Capacity and Separation Window -- 10.2.4 Coupling Novel Gas‐Phase Fragmentation Techniques to CZE-MS/MS for TDP -- 10.2.5 Electrophoretic Mobility Prediction of Proteoforms -- 10.3 Applications of CZE-MS‐Based TDP -- 10.3.1 Delineation of Proteoforms of Complex Proteomes, Disease Biomarkers, and Biopharmaceuticals -- 10.3.2 CZE-MS for Native TDP -- 10.4 Conclusions and Perspectives -- Acknowledgments -- References -- Chapter 11 CE-MS Methods for the Characterization of Monoclonal Antibodies -- 11.1 Introduction -- 11.2 mAb Characterization Approaches -- 11.3 Applications -- 11.3.1 Primary Structure Characterization of Monoclonal Antibodies -- 11.3.1.1 Analytical Workflow -- 11.3.1.2 Amino Acid Sequence Characterization Using CE-MS(/MS) -- 11.3.1.3 PTMs Characterization and Relative Quantification Using CE-MS(/MS) -- 11.3.1.4 Glycosylation Determination Using CE-MS(/MS) -- 11.3.2 Middle‐Up/Middle‐Down Analysis -- 11.3.2.1 Analytical Workflow -- 11.3.2.2 mAb Analysis Using Middle‐Up Strategy -- 11.3.2.3 mAb Analysis Using Middle-Down Strategy -- 11.3.3 Intact Analysis -- 11.3.3.1 Analytical Workflow -- 11.3.3.2 mAb Analysis in Denaturing Conditions Using CE-MS -- 11.3.3.3 mAb Analysis in Native Conditions Using CE-MS -- 11.3.4 Automation: Future of CE-MS for mAb Analysis -- 11.4 Conclusion -- References. Chapter 12 CE and CE-MS Approaches for Glycan Analysis -- 12.1 The Importance of Glycosylation -- 12.2 Capillary Electrophoresis in Analytical Glycomics -- 12.2.1 Sample Preparation for CE‐Based Glycan Analysis -- 12.2.2 Analysis of Oligosaccharides from Biological Samples -- 12.2.3 Structural Elucidation of Carbohydrates: The GU Value Approach -- 12.2.4 LIF Sensitivity and Quantification -- 12.3 CE-MS of Oligosaccharides -- 12.3.1 Major Parameters to Set the ESI for CE-MS of Derivatized Oligosaccharides -- 12.3.2 CE-MS for Quantitative Carbohydrate Analysis -- 12.3.3 CE-MS for Glycomic Studies -- 12.4 Conclusions and Future Prospective -- Acknowledgment -- References -- Chapter 13 CE-MS Approaches for Glyco(proteo)mic Analysis -- 13.1 Introduction -- 13.1.1 N‐Linked Glycosylation -- 13.1.2 O‐Linked Glycosylation -- 13.1.3 Glycosylation Workflows -- 13.1.4 Analytical Approaches -- 13.1.5 CE-MS Interfaces -- 13.2 Glycan Analysis by CE-MS -- 13.2.1 Glycan Derivatization Strategies -- 13.3 Glycopeptide Analysis -- 13.3.1 Sample Treatment -- 13.3.2 Separation Conditions -- 13.3.3 Applications -- 13.4 Protein Analysis -- 13.4.1 Sample Treatment -- 13.4.2 Separation Conditions -- 13.4.3 Applications -- 13.5 Conclusions and Outlook -- Acknowledgments -- List of Abbreviations -- References -- Index -- EULA. |
Record Nr. | UNINA-9910644087903321 |
Hoboken, New Jersey : , : John Wiley & Sons, , [2023] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Capillary electrophoresis -- mass spectrometry for proteomics and metabolomics : principles and applications / / edited by Rawi Ramautar and David D. Y. Chen |
Pubbl/distr/stampa | Hoboken, New Jersey : , : John Wiley & Sons, , [2023] |
Descrizione fisica | 1 online resource (403 pages) |
Disciplina | 541.372 |
Soggetto topico | Capillary electrophoresis |
ISBN |
3-527-83309-9
3-527-83308-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Capillary Electrophoresis-Mass Spectrometry Interfacing: Principles and Recent Developments -- 1.1 Introduction -- 1.2 General Considerations of CE-ESI-MS -- 1.2.1 Electrospray Ionization -- 1.2.2 Electrical Circuit in CE-ESI-MS -- 1.2.3 CE Modes and Conditions in CE-MS -- 1.3 Sheath Liquid Interfaces -- 1.3.1 Coaxial Sheath‐Flow ESI-MS Interface -- 1.3.2 Nanoflow Sheath Liquid ESI-MS Interface -- 1.4 Sheathless Interfaces -- 1.4.1 Porous‐Tip Interface -- 1.4.2 Other Sheathless Interfaces -- 1.5 Other CE-ESI-MS Interfaces -- 1.5.1 Liquid Junction -- 1.5.2 Interface‐Free CE-MS -- 1.6 Microchip Electrophoresis-MS Interfaces -- 1.7 Alternative Ionization Techniques for CE-MS -- 1.7.1 CE and MCE Combined with MALDI-MS -- 1.7.2 CE-ICP-MS -- 1.8 Concluding Remarks and Outlook -- List of Abbreviations -- References -- Chapter 2 Data Analysis Strategies in CE-MS for Metabolomics -- 2.1 Introduction -- 2.2 The Annotation Challenge in CE-MS‐Based Untargeted Metabolomics -- 2.2.1 Peak Picking in CE-MS Metabolomics -- 2.2.2 Alignment Approaches -- 2.2.3 μeff Transformation -- 2.2.3.1 Historical Evolution and Current State -- 2.2.3.2 Quantitative Aspects of the Use of Mobilograms -- 2.2.3.3 Technical Considerations of the μeff Transformation -- 2.2.4 Reproducibility and Exchange of μeff Information Using Libraries -- 2.2.5 Interlaboratory Reproducibility -- 2.2.6 ROMANCE -- 2.2.7 Ion Mobility -- 2.3 Data Pretreatment -- 2.3.1 Area Normalization -- 2.3.2 Analytical Quality Monitoring -- 2.3.3 Data Filtering -- 2.4 Data Treatment -- 2.5 Concluding Remarks -- Acknowledgment -- References -- Chapter 3 Data‐Processing Workflow for Relative Quantification from Label‐Free and Isobaric Labeling‐Based Untargeted Shotgun Proteomics: From Database Search to Differential Expression Analysis.
3.1 Introduction -- 3.2 Spectra Acquisition and Database Search -- 3.2.1 Parameters Affecting Sequence Database Search -- 3.2.1.1 Database Selection -- 3.2.1.2 Enzyme Specificity and Missed Cleavages -- 3.2.1.3 Posttranslational Modifications -- 3.2.1.4 Precursor Mass Tolerance -- 3.2.2 Target-Decoy Search Strategy for False Discovery Rate Estimation -- 3.2.3 Database Search Engines -- 3.2.3.1 SEQUEST -- 3.2.3.2 Mascot -- 3.2.3.3 Multiple Search Engines -- 3.2.4 Protein Inference -- 3.3 Relative Protein Quantification -- 3.3.1 Filtering -- 3.3.2 Missing Value Imputation -- 3.3.2.1 Imputation Methods -- 3.3.2.2 Comparative Studies -- 3.3.2.3 Normalization -- 3.3.3 Summarization -- 3.3.4 Differential Expression Analysis -- 3.4 Conclusions -- References -- Chapter 4 Data Processing in Metabolomics Capillary Electrophoresis-Mass Spectrometry -- 4.1 Data Extraction and the Interpretation of the Extracted Data -- 4.2 Data Preprocessing -- 4.2.1 Handling Missing Values -- 4.2.2 Normalization -- 4.2.3 Transformation -- 4.2.4 Scaling -- 4.3 Statistical Analysis -- 4.3.1 Two‐Sample T‐Test -- 4.3.2 Principal Component Analysis (PCA) -- 4.3.3 Partial Least‐Squares Discriminant Analysis (PLS-DA) -- 4.3.4 Support Vector Machine -- 4.3.5 Logistic Regression -- 4.3.6 Random Forest Model -- 4.3.7 Evaluation of Classification Models -- 4.4 Metabolite Identification -- References -- Chapter 5 Utility and Advances of Capillary Electrophoresis-Mass Spectrometry for Metabolomics -- 5.1 Introduction -- 5.2 Technological Developments -- 5.2.1 Improving Sensitivity -- 5.2.2 Increasing Metabolome Coverage -- 5.2.3 Increasing Annotation Capacity -- 5.2.4 Tackling Anionic Profiling -- 5.2.5 Increasing Sample Throughput -- 5.3 Applications -- 5.3.1 Biomedical Samples -- 5.3.2 Microbial Extracts -- 5.3.3 Plants -- 5.4 Concluding Remarks -- Acknowledgment -- Conflict of Interest. References -- Chapter 6 Comprehensive Lipid Profiling by Multisegment Injection-Nonaqueous Capillary Electrophoresis-Mass Spectrometry: Expanding Coverage Beyond Hydrophilic Metabolites -- 6.1 The Early Origins of Lipidomics -- 6.2 Major Instrumental Platforms in Lipidomics: The Role of Separation Science -- 6.3 NACE-MS: An Emerging Separation Platform for Lipidomics? -- 6.4 Multiplexed Separations for Fatty Acids by MSI-NACE-MS -- 6.5 Comprehensive Lipid Profiling Strategies by MSI-NACE-MS -- 6.6 Future Perspectives and Summary -- References -- Chapter 7 Strategies for Identification of Modified Amino Acids with CE-MS in Metabolomics -- 7.1 Introduction -- 7.1.1 Post‐Translational Modifications and Modified Amino Acids -- 7.1.2 Modified Amino Acids as Biomarkers of Pathologies -- 7.2 Methods for the Detection of Modified Amino Acids -- 7.3 Capillary Electrophoresis Coupled to Mass Spectrometry to Analyze Modified Amino Acids -- 7.3.1 Applications of CE-MS for Analysis of Modified Amino Acids -- 7.4 Recent Developments to Enhance and Facilitate the Annotation Process in CE-MS -- Acknowledgments -- References -- Chapter 8 CE-MS Approaches for Single‐Cell Metabolomics -- 8.1 Introduction -- 8.2 Techniques for Single‐Cell Metabolome Analysis -- 8.2.1 Highly Sensitive CE-MS Interfacing -- 8.2.2 Online Sample Preconcentration Techniques -- 8.2.3 Isolation of Single Cells -- 8.3 Application to Single‐Cell Metabolome Analysis -- 8.3.1 Metabolome Analysis of Large Single Cells with Highly Sensitive Interface -- 8.3.2 Single‐Cell Metabolome Analysis with Highly Sensitive Interface and OSP Method -- 8.3.3 Single‐Cell Metabolome Analysis by Online Sampling and Highly Sensitive Interface -- 8.4 Conclusions -- References -- Chapter 9 CE-MS Approaches for Peptidomics -- 9.1 Introduction -- 9.2 Sample Preparation -- 9.3 CE-MS -- 9.3.1 Basic Characterization. 9.3.2 Peptide Identification -- 9.3.3 Peptide Quantitation -- 9.4 Applications -- 9.4.1 Search, Identification, and Determination of Biomarkers -- 9.4.2 Food Peptidomics -- 9.4.3 Other Applications -- 9.5 Conclusions -- Acknowledgments -- List of Abbreviations -- References -- Chapter 10 Capillary Zone Electrophoresis-Mass Spectrometry for Top‐Down Proteomics: Technological Development and Biological Applications -- 10.1 Introduction -- 10.2 Technological Development -- 10.2.1 CE-MS Interface -- 10.2.2 Capillary Coating -- 10.2.3 Sample Loading Capacity and Separation Window -- 10.2.4 Coupling Novel Gas‐Phase Fragmentation Techniques to CZE-MS/MS for TDP -- 10.2.5 Electrophoretic Mobility Prediction of Proteoforms -- 10.3 Applications of CZE-MS‐Based TDP -- 10.3.1 Delineation of Proteoforms of Complex Proteomes, Disease Biomarkers, and Biopharmaceuticals -- 10.3.2 CZE-MS for Native TDP -- 10.4 Conclusions and Perspectives -- Acknowledgments -- References -- Chapter 11 CE-MS Methods for the Characterization of Monoclonal Antibodies -- 11.1 Introduction -- 11.2 mAb Characterization Approaches -- 11.3 Applications -- 11.3.1 Primary Structure Characterization of Monoclonal Antibodies -- 11.3.1.1 Analytical Workflow -- 11.3.1.2 Amino Acid Sequence Characterization Using CE-MS(/MS) -- 11.3.1.3 PTMs Characterization and Relative Quantification Using CE-MS(/MS) -- 11.3.1.4 Glycosylation Determination Using CE-MS(/MS) -- 11.3.2 Middle‐Up/Middle‐Down Analysis -- 11.3.2.1 Analytical Workflow -- 11.3.2.2 mAb Analysis Using Middle‐Up Strategy -- 11.3.2.3 mAb Analysis Using Middle-Down Strategy -- 11.3.3 Intact Analysis -- 11.3.3.1 Analytical Workflow -- 11.3.3.2 mAb Analysis in Denaturing Conditions Using CE-MS -- 11.3.3.3 mAb Analysis in Native Conditions Using CE-MS -- 11.3.4 Automation: Future of CE-MS for mAb Analysis -- 11.4 Conclusion -- References. Chapter 12 CE and CE-MS Approaches for Glycan Analysis -- 12.1 The Importance of Glycosylation -- 12.2 Capillary Electrophoresis in Analytical Glycomics -- 12.2.1 Sample Preparation for CE‐Based Glycan Analysis -- 12.2.2 Analysis of Oligosaccharides from Biological Samples -- 12.2.3 Structural Elucidation of Carbohydrates: The GU Value Approach -- 12.2.4 LIF Sensitivity and Quantification -- 12.3 CE-MS of Oligosaccharides -- 12.3.1 Major Parameters to Set the ESI for CE-MS of Derivatized Oligosaccharides -- 12.3.2 CE-MS for Quantitative Carbohydrate Analysis -- 12.3.3 CE-MS for Glycomic Studies -- 12.4 Conclusions and Future Prospective -- Acknowledgment -- References -- Chapter 13 CE-MS Approaches for Glyco(proteo)mic Analysis -- 13.1 Introduction -- 13.1.1 N‐Linked Glycosylation -- 13.1.2 O‐Linked Glycosylation -- 13.1.3 Glycosylation Workflows -- 13.1.4 Analytical Approaches -- 13.1.5 CE-MS Interfaces -- 13.2 Glycan Analysis by CE-MS -- 13.2.1 Glycan Derivatization Strategies -- 13.3 Glycopeptide Analysis -- 13.3.1 Sample Treatment -- 13.3.2 Separation Conditions -- 13.3.3 Applications -- 13.4 Protein Analysis -- 13.4.1 Sample Treatment -- 13.4.2 Separation Conditions -- 13.4.3 Applications -- 13.5 Conclusions and Outlook -- Acknowledgments -- List of Abbreviations -- References -- Index -- EULA. |
Record Nr. | UNINA-9910830168203321 |
Hoboken, New Jersey : , : John Wiley & Sons, , [2023] | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|