Chemicals and fuels from bio-based building blocks / / edited by Fabrizio Cavani [and three others]
| Chemicals and fuels from bio-based building blocks / / edited by Fabrizio Cavani [and three others] |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (861 p.) |
| Soggetto topico |
Biomass
Biomass energy Renewable energy sources Green chemistry Biomass chemicals Polymerization - Environmental aspects Biocatalysis Biomass - Refining |
| ISBN |
3-527-69820-5
3-527-69819-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Title Page; Copyright; Table of Contents; List of Contributors; Preface; Volume 1; Part I: Drop-in Bio-Based Chemicals; Chapter 1: Olefins from Biomass; 1.1 Introduction; 1.2 Olefins from Bioalcohols; 1.3 Alternative Routes to Bio-Olefins; 1.4 Conclusions; References; Chapter 2: Aromatics from Biomasses: Technological Options for Chemocatalytic Transformations; 2.1 The Synthesis of Bioaromatics; 2.2 The Synthesis of Bio-p-Xylene, a Precursor for Bioterephthalic Acid; 2.3 The Synthesis of Bioterephthalic Acid without the Intermediate Formation of p-Xylene
2.4 Technoeconomic and Environmental Assessment of Bio-p-Xylene ProductionReferences; Chapter 3: Isostearic Acid: A Unique Fatty Acid with Great Potential; 3.1 Introduction; 3.2 Biorefinery and Related Concepts; 3.3 Sustainability of Oils and Fats for Industrial Applications; 3.4 Fatty Acids; 3.5 Polymerization of Fatty Acids; 3.6 ISAC; 3.7 Other Branched Chain Fatty Acids; 3.8 Properties of ISAC; 3.9 Applications of ISAC; 3.10 Selective Routes for the Production of ISAC; 3.11 Summary and Conclusions; Acknowledgments; References Chapter 4: Biosyngas and Derived Products from Gasification and Aqueous Phase Reforming4.1 Introduction; 4.2 Biomass Gasification; 4.3 Aqueous Phase Reforming; References; Chapter 5: The Hydrogenation of Vegetable Oil to Jet and Diesel Fuels in a Complex Refining Scenario; 5.1 Introduction; 5.2 The Feedstock; 5.3 Hydroconversion Processes of Vegetable Oils and Animal Fats; 5.4 Chemistry of Triglycerides Hydroconversion; 5.5 Life Cycle Assessment and Emission; 5.6 The Green Refinery Project; 5.7 Conclusions; References; Part II: Bio-Monomers Chapter 6: Synthesis of Adipic Acid Starting from Renewable Raw Materials6.1 Introduction; 6.2 Challenges for Bio-Based Chemicals Production; 6.3 Choice of Adipic Acid as Product Target by Rennovia; 6.4 Conventional and Fermentation-Based Adipic Acid Production Technologies; 6.5 Rennovia's Bio-Based Adipic Acid Production Technology; 6.6 Step 1: Selective Oxidation of Glucose to Glucaric Acid; 6.7 Step 2: Selective Hydrodeoxygenation of Glucaric Acid to Adipic Acid; 6.8 Current Status of Rennovia's Bio-Based Adipic Acid Process Technology 6.9 Bio- versus Petro-Based Adipic Acid Production Economics6.10 Life Cycle Assessment; 6.11 Conclusions; References; Chapter 7: Industrial Production of Succinic Acid; 7.1 Introduction; 7.2 Market and Applications; 7.3 Technology; 7.4 Life Cycle Analysis; 7.5 Conclusion; References; Chapter 8: 2,5-Furandicarboxylic Acid Synthesis and Use; 8.1 Introduction; 8.2 Synthesis of 2,5-Furandicarboxylic Acid by Oxidation of HMF; 8.3 Synthesis of 2,5-Furandicarboxylic Acid from Carbohydrates and Furfural; 8.4 2,5-Furandicarboxylic Acid-Derived Surfactants and Plasticizers 8.5 2,5-Furandicarboxylic Acid-Derived Polymers |
| Record Nr. | UNINA-9910136413403321 |
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Micro- and nanosystems for biotechnology / / edited by J. Christopher Love
| Micro- and nanosystems for biotechnology / / edited by J. Christopher Love |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (305 p.) |
| Collana | Advanced biotechnology |
| Soggetto topico |
Biotechnology
Nanotechnology Microtechnology |
| ISBN |
3-527-80132-4
3-527-80129-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; List of Contributors; About the Series Editors; Preface; Part I Microsystems for Single-Cell Analysis; Chapter 1 Types of Clinical Samples and Cellular Enrichment Strategies; 1.1 Introduction; 1.2 Types of Clinical Samples; 1.2.1 Solid Clinical Samples; 1.2.1.1 Cellular Subtypes Found in Solid Clinical Samples; 1.2.2 Liquid Clinical Samples and Cellular Subtypes; 1.2.2.1 Blood; 1.2.2.2 Bone Marrow; 1.2.2.3 Placental or Umbilical Cord Blood; 1.2.2.4 Urine; 1.2.2.5 Cerebrospinal Fluid (CSF); 1.2.2.6 Saliva
1.3 Sample Processing and Conventional Methods of Cell Enrichment1.3.1 Processing Solid Clinical Samples; 1.3.1.1 Processing Liquid Samples; 1.3.2 Cell Enrichment; 1.3.2.1 Laser Capture Microdissection (LCM); 1.3.2.2 Density Gradient Centrifugation; 1.3.2.3 Fluorescence-Activated Cell Sorting (FACS); 1.3.2.4 Magnetic Activated Cell Sorting (MACS); 1.3.2.5 CellSearchTM; 1.4 Microscale/Nanoscale Devices for Cellular Enrichment; 1.4.1 Filtration Approaches; 1.4.2 Hydrodynamic Mechanisms; 1.4.3 Surface Treatments; 1.4.4 Magnetophoresis; 1.4.5 Electrophoresis; 1.4.6 Acoustophoresis 1.4.7 Optical Tweezers/Traps1.5 Conclusion; References; Chapter 2 Genome-Wide Analysis of Single Cells and the Role of Microfluidics; 2.1 Motivation for Single-Cell Analysis of Genomes and Transcriptomes; 2.2 Single-Cell Genomics; 2.2.1 Major Technical Challenges; 2.2.2 Approaches to Single-Cell Genomics; 2.2.3 The Application and Impact of Microfluidics in Single-Cell Genomics; 2.3 Single-Cell Transcriptomics; 2.3.1 Major Technical Challenges; 2.3.2 Approaches to Single-Cell Transcriptomics; 2.3.3 Application and Impact of Microfluidics in Single-Cell Transcriptomics 2.4 The Future of Genome-Wide Single-Cell Analysis with Microfluidics2.4.1 Recent Advances in the Scalability of Single-Cell Analysis using Microfluidics; 2.4.2 How Microfluidics will Expand the Application-Space for Single-Cell Analysis; 2.4.3 Outstanding Hurdles for Genome-Wide Analysis of Single Cells; 2.4.4 Prospects for Clinical Applications of Microfluidic Single-Cell Analysis; Keywords and Definitions; References; Chapter 3 Cellular Immunophenotyping: Industrial Technologies and Emerging Tools; 3.1 Cellular Immune Status and Immunophenotyping; 3.2 Surface Marker Phenotyping 3.2.1 Multicolor Flow Cytometry3.2.2 Commercial Flow Cytometers; 3.2.3 High-Content Imaging Cytometry; 3.2.4 Current Limitations and Further Development of Flow Cytometry; 3.3 Functional Phenotyping; 3.3.1 ELISpot Technologies; 3.3.2 Multiplexed Immunoassays; 3.3.3 Emerging Single-Cell Technologies; 3.4 Conclusion; Keywords and Definitions; References; Chapter 4 Microsystem Assays for Studying the Interactions between Single Cells; 4.1 Introduction; 4.2 Advantages of Single-Cell Analysis over Conventional Assay Systems; 4.3 Analysis of Cell-Cell Communication between Pairs of Single Cells 4.3.1 Integrated Microfluidic Coculture Systems and Microwell Arrays |
| Record Nr. | UNINA-9910136458303321 |
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Micro- and nanosystems for biotechnology / / edited by J. Christopher Love
| Micro- and nanosystems for biotechnology / / edited by J. Christopher Love |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (305 p.) |
| Collana | Advanced biotechnology |
| Soggetto topico |
Biotechnology
Nanotechnology Microtechnology |
| ISBN |
3-527-80132-4
3-527-80129-4 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; List of Contributors; About the Series Editors; Preface; Part I Microsystems for Single-Cell Analysis; Chapter 1 Types of Clinical Samples and Cellular Enrichment Strategies; 1.1 Introduction; 1.2 Types of Clinical Samples; 1.2.1 Solid Clinical Samples; 1.2.1.1 Cellular Subtypes Found in Solid Clinical Samples; 1.2.2 Liquid Clinical Samples and Cellular Subtypes; 1.2.2.1 Blood; 1.2.2.2 Bone Marrow; 1.2.2.3 Placental or Umbilical Cord Blood; 1.2.2.4 Urine; 1.2.2.5 Cerebrospinal Fluid (CSF); 1.2.2.6 Saliva
1.3 Sample Processing and Conventional Methods of Cell Enrichment1.3.1 Processing Solid Clinical Samples; 1.3.1.1 Processing Liquid Samples; 1.3.2 Cell Enrichment; 1.3.2.1 Laser Capture Microdissection (LCM); 1.3.2.2 Density Gradient Centrifugation; 1.3.2.3 Fluorescence-Activated Cell Sorting (FACS); 1.3.2.4 Magnetic Activated Cell Sorting (MACS); 1.3.2.5 CellSearchTM; 1.4 Microscale/Nanoscale Devices for Cellular Enrichment; 1.4.1 Filtration Approaches; 1.4.2 Hydrodynamic Mechanisms; 1.4.3 Surface Treatments; 1.4.4 Magnetophoresis; 1.4.5 Electrophoresis; 1.4.6 Acoustophoresis 1.4.7 Optical Tweezers/Traps1.5 Conclusion; References; Chapter 2 Genome-Wide Analysis of Single Cells and the Role of Microfluidics; 2.1 Motivation for Single-Cell Analysis of Genomes and Transcriptomes; 2.2 Single-Cell Genomics; 2.2.1 Major Technical Challenges; 2.2.2 Approaches to Single-Cell Genomics; 2.2.3 The Application and Impact of Microfluidics in Single-Cell Genomics; 2.3 Single-Cell Transcriptomics; 2.3.1 Major Technical Challenges; 2.3.2 Approaches to Single-Cell Transcriptomics; 2.3.3 Application and Impact of Microfluidics in Single-Cell Transcriptomics 2.4 The Future of Genome-Wide Single-Cell Analysis with Microfluidics2.4.1 Recent Advances in the Scalability of Single-Cell Analysis using Microfluidics; 2.4.2 How Microfluidics will Expand the Application-Space for Single-Cell Analysis; 2.4.3 Outstanding Hurdles for Genome-Wide Analysis of Single Cells; 2.4.4 Prospects for Clinical Applications of Microfluidic Single-Cell Analysis; Keywords and Definitions; References; Chapter 3 Cellular Immunophenotyping: Industrial Technologies and Emerging Tools; 3.1 Cellular Immune Status and Immunophenotyping; 3.2 Surface Marker Phenotyping 3.2.1 Multicolor Flow Cytometry3.2.2 Commercial Flow Cytometers; 3.2.3 High-Content Imaging Cytometry; 3.2.4 Current Limitations and Further Development of Flow Cytometry; 3.3 Functional Phenotyping; 3.3.1 ELISpot Technologies; 3.3.2 Multiplexed Immunoassays; 3.3.3 Emerging Single-Cell Technologies; 3.4 Conclusion; Keywords and Definitions; References; Chapter 4 Microsystem Assays for Studying the Interactions between Single Cells; 4.1 Introduction; 4.2 Advantages of Single-Cell Analysis over Conventional Assay Systems; 4.3 Analysis of Cell-Cell Communication between Pairs of Single Cells 4.3.1 Integrated Microfluidic Coculture Systems and Microwell Arrays |
| Record Nr. | UNINA-9910810800403321 |
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Receptor biology / / Michael F. Roberts and Anne E. Kruhchten
| Receptor biology / / Michael F. Roberts and Anne E. Kruhchten |
| Autore | Roberts Michael F. |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (478 p.) |
| Soggetto topico |
Cell receptors
Nuclear receptors (Biochemistry) Binding sites (Biochemistry) Ligands (Biochemistry) |
| Soggetto genere / forma | Electronic books. |
| ISBN | 3-527-80015-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Title Page; Copyright; Dedication; Table of Contents; Acknowledgments; Part I: Introduction; Chapter 1: Introduction; 1.1 Receptors and Signaling; 1.2 Types of Receptors and Hormones; 1.3 Receptors Are the Chemical Expression of Reality; Chapter 2: The Origins of Chemical Thinking; 2.1 Overview of Early Pharmacological History; 2.2 Modern Pharmacology; 2.3 Phylogenetics of Signaling; Part II: Fundamentals; Chapter 3: Membranes and Proteins; 3.1 Membranes; 3.2 The Nature and Function of Proteins; Chapter 4: Hormones as First Messengers; 4.1 Hormones and Cellular Communication
4.2 Types of Hormones4.3 Vertebrate Hormones and Transmitters; 4.4 Analgesics and Venoms as Receptor Ligands; Chapter 5: Receptor Theory; 5.1 The Materialization of Receptors; 5.2 Receptor Mechanisms; 5.3 Binding Theory; 5.4 Visualizing Receptor Structure and Function; 5.5 Proteomics Approaches to Receptor Efficacy; 5.6 Physical Factors Affecting Receptor Binding; Part III: Receptor Types and Function; Chapter 6: Transduction I: Ion Channels and Transporters; 6.1 Introduction; 6.2 Small Molecule Channels; 6.3 Transporters; 6.4 Major Intrinsic Proteins; 6.5 Ligand-Gated Ion Channels Chapter 7: Transduction II: G-Protein-Coupled Receptors7.1 Introduction; 7.2 Families of G-Protein-Coupled Receptors; 7.3 Transduction Mechanisms; 7.4 The Major Families of G Protein-Coupled Receptors; Chapter 8: Transduction III: Receptor Kinases and Immunoglobulins; 8.1 Protein Kinases; 8.2 Receptors for Cell Division and Metabolism; 8.3 Receptor Serine/Threonine Kinases; 8.4 The Guanylyl Cyclase Receptor Subfamily - Natriuretic Peptide Receptors; 8.5 Non-Kinase Molecules - LDL Receptors; 8.6 Cell-Cell Contact Signaling; 8.7 Immune System Receptors, Antibodies, and Cytokines Chapter 9: Transduction IV: Nuclear Receptors9.1 Introduction; 9.2 Genomic Actions of Nuclear Receptors; 9.3 Actions of Receptor Antagonists; 9.4 Non-Traditional Actions of Steroid-Like Hormones and Their Receptors; Part IV: Applications; Chapter 10: Signaling Complexity; 10.1 Introduction; 10.2 Experimental Determination of Signaling Cascades; 10.3 Transduction across the Membrane; 10.4 Complexity in Cross Talk - Roles of PIP3, Akt, and PDK1; 10.5 Role in Cancer; 10.6 Signaling Mediated by Gas Molecules; Chapter 11: Cellular Interactions in Development; 11.1 Introduction 11.2 The Origins of Multicellularity11.3 The Origin of Symmetry and Axes; 11.4 Fertilization and Organization of the Multicellular Body Plan; 11.5 Differentiation of Triploblastic Embryos - Organogenesis; 11.6 Programmed Cell Death (Apoptosis); Chapter 12: Receptor Mechanisms in Disease Processes; 12.1 Genetic Basis for Receptor Function; 12.2 Receptor Pathologies; 12.3 Signaling Mutations Leading to Cancer; Chapter 13: Receptors and the Mind; 13.1 Origins of Behavior; 13.2 Nervous Systems; 13.3 Animal Memory: Invertebrates; 13.4 Animal Memory: Vertebrates 13.5 Receptors and Behavior: Addiction, Tolerance, and Dependence |
| Record Nr. | UNINA-9910466108203321 |
Roberts Michael F.
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Receptor biology / / Michael F. Roberts and Anne E. Kruhchten
| Receptor biology / / Michael F. Roberts and Anne E. Kruhchten |
| Autore | Roberts Michael F. |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (478 pages) : illustrations (some color) |
| Soggetto topico |
Binding sites (Biochemistry)
Cell receptors Ligands (Biochemistry) Nuclear receptors (Biochemistry) |
| ISBN |
3-527-80017-4
3-527-80015-8 |
| Classificazione |
463.6
571.6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910796090903321 |
Roberts Michael F.
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Receptor biology / / Michael F. Roberts and Anne E. Kruhchten
| Receptor biology / / Michael F. Roberts and Anne E. Kruhchten |
| Autore | Roberts Michael F. |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] |
| Descrizione fisica | 1 online resource (478 pages) : illustrations (some color) |
| Soggetto topico |
Binding sites (Biochemistry)
Cell receptors Ligands (Biochemistry) Nuclear receptors (Biochemistry) |
| ISBN |
3-527-80017-4
3-527-80015-8 |
| Classificazione |
463.6
571.6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910822760103321 |
Roberts Michael F.
|
||
| Weinheim, Germany : , : Wiley-VCH Verlag GmBH & Company KGaA, , [2016] | ||
| Lo trovi qui: Univ. Federico II | ||
| ||