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Expression and analysis of recombinant ion channels [[electronic resource] ] : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise
| Expression and analysis of recombinant ion channels [[electronic resource] ] : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise |
| Pubbl/distr/stampa | Weinheim ; ; [Chichester], : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (305 p.) |
| Disciplina | 572.3 |
| Altri autori (Persone) |
ClareJeffrey J
TreziseDerek J |
| Soggetto topico |
Ion channels
Biological transport, Active |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-72342-4
9786610723423 3-527-60809-5 3-527-60793-5 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Expression and Analysis of Recombinant Ion Channels; Contents; Preface; List of Contributors; Color Plates; 1 Expression of Ion Channels in Xenopus Oocytes; 1.1 Introduction; 1.2 Advantages and Disadvantages of Xenopus Oocytes; 1.3 Procedures for Using Oocytes; 1.4 Types of Analyses; 1.4.1 Electrophysiological Analysis; 1.4.1.1 Two-electrode Whole Cell Voltage-clamp; 1.4.1.2 Cut-open Oocyte Voltage-clamp; 1.4.1.3 Macropatch Clamp; 1.4.1.4 Single Channel Analysis; 1.4.2 Biochemical Analysis; 1.4.3 Compound Screening; 1.4.3.1 Serial Recording Using the Roboocyte
1.4.3.2 Parallel Recording Using the OpusXpress1.5 Examples of Use; 1.5.1 Characterization of cDNA Clones for a Channel; 1.5.2 Structure-Function Correlations; 1.5.3 Studies of Human Disease Mutations; 1.6 Conclusions; Acknowledgments; References; 2 Molecular Biology Techniques for Structure - Function Studies of Ion Channels; 2.1 Introduction; 2.2 Methods for cDNA Subcloning; 2.2.1 Conventional Sub-cloning Using Restriction Enzymes and DNA Ligase; 2.2.2 PCR-based cDNA Sub-cloning; 2.2.3 Sub-cloning cDNA through Site-specific Recombination; 2.3 Generation of Chimeric Channel cDNAs 2.3.1 Use of Restriction Enzymes to Generate Chimeric Channel cDNAs2.3.2 PCR-mediated Overlap Extension for Chimera Generation; 2.3.3 PCR-mediated Integration or Replacement of cDNA Fragments; 2.4 Site-directed Mutagenesis; 2.4.1 Examples of the Use of Site-directed Mutagenesis; 2.4.2 Modification of the QuikChange Method for the Replacement of cDNA Fragments; 2.5 Epitope-tagged Channels and Fusion Partners; 2.6 Channel Subunit Concatamers; 2.7 Concluding Remarks; References; 3 Unnatural Amino Acids as Probes of Ion Channel Structure - Function and Pharmacology; 3.1 Introduction 3.2 Unnatural Amino Acid Mutagenesis Methodology3.3 Unnatural Amino Acid Mutagenesis for Ion Channel Studies; 3.4 Structure-Function Example Studies; 3.4.1 Nicotinic Acetylcholine Receptor; 3.4.2 Drug Interactions with the hERG Voltage-gated Potassium Ion Channel; 3.5 Other Uses of Unnatural Amino Acids as Probes of Protein Structure and Function; 3.6 Conclusions; Acknowledgements; References; 4 Functional Expression of Ion Channels in Mammalian Systems; 4.1 Introduction; 4.2 cDNA Cloning and Manipulation; 4.3 Choice of Host Cell Background 4.4 Post-translational Processing of Heterologous Expressed Ion Channels4.5 Cytotoxicity; 4.6 Transient Expression Systems; 4.6.1 "Standard" Transient Expression; 4.6.2 Viral Expression Systems; 4.7 Stable Expression of Ion Channels; 4.7.1 Bicistronic Expression Systems; 4.7.2 Stable Expression of Multiple Subunits; 4.7.3 Inducible Expression; 4.8 Summary; Acknowledgements; References; 5 Analysis of Electrophysiological Data; 5.1 Overview; 5.2 Introduction; 5.3 Expression Systems and Related Recording Techniques; 5.3.1 Expression in Xenopus Oocytes; 5.3.2 Expression in Mammalian Cells 5.3.3 Leak and Capacitance Subtraction |
| Record Nr. | UNINA-9910143961803321 |
| Weinheim ; ; [Chichester], : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Expression and analysis of recombinant ion channels [[electronic resource] ] : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise
| Expression and analysis of recombinant ion channels [[electronic resource] ] : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise |
| Pubbl/distr/stampa | Weinheim ; ; [Chichester], : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (305 p.) |
| Disciplina | 572.3 |
| Altri autori (Persone) |
ClareJeffrey J
TreziseDerek J |
| Soggetto topico |
Ion channels
Biological transport, Active |
| ISBN |
1-280-72342-4
9786610723423 3-527-60809-5 3-527-60793-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Expression and Analysis of Recombinant Ion Channels; Contents; Preface; List of Contributors; Color Plates; 1 Expression of Ion Channels in Xenopus Oocytes; 1.1 Introduction; 1.2 Advantages and Disadvantages of Xenopus Oocytes; 1.3 Procedures for Using Oocytes; 1.4 Types of Analyses; 1.4.1 Electrophysiological Analysis; 1.4.1.1 Two-electrode Whole Cell Voltage-clamp; 1.4.1.2 Cut-open Oocyte Voltage-clamp; 1.4.1.3 Macropatch Clamp; 1.4.1.4 Single Channel Analysis; 1.4.2 Biochemical Analysis; 1.4.3 Compound Screening; 1.4.3.1 Serial Recording Using the Roboocyte
1.4.3.2 Parallel Recording Using the OpusXpress1.5 Examples of Use; 1.5.1 Characterization of cDNA Clones for a Channel; 1.5.2 Structure-Function Correlations; 1.5.3 Studies of Human Disease Mutations; 1.6 Conclusions; Acknowledgments; References; 2 Molecular Biology Techniques for Structure - Function Studies of Ion Channels; 2.1 Introduction; 2.2 Methods for cDNA Subcloning; 2.2.1 Conventional Sub-cloning Using Restriction Enzymes and DNA Ligase; 2.2.2 PCR-based cDNA Sub-cloning; 2.2.3 Sub-cloning cDNA through Site-specific Recombination; 2.3 Generation of Chimeric Channel cDNAs 2.3.1 Use of Restriction Enzymes to Generate Chimeric Channel cDNAs2.3.2 PCR-mediated Overlap Extension for Chimera Generation; 2.3.3 PCR-mediated Integration or Replacement of cDNA Fragments; 2.4 Site-directed Mutagenesis; 2.4.1 Examples of the Use of Site-directed Mutagenesis; 2.4.2 Modification of the QuikChange Method for the Replacement of cDNA Fragments; 2.5 Epitope-tagged Channels and Fusion Partners; 2.6 Channel Subunit Concatamers; 2.7 Concluding Remarks; References; 3 Unnatural Amino Acids as Probes of Ion Channel Structure - Function and Pharmacology; 3.1 Introduction 3.2 Unnatural Amino Acid Mutagenesis Methodology3.3 Unnatural Amino Acid Mutagenesis for Ion Channel Studies; 3.4 Structure-Function Example Studies; 3.4.1 Nicotinic Acetylcholine Receptor; 3.4.2 Drug Interactions with the hERG Voltage-gated Potassium Ion Channel; 3.5 Other Uses of Unnatural Amino Acids as Probes of Protein Structure and Function; 3.6 Conclusions; Acknowledgements; References; 4 Functional Expression of Ion Channels in Mammalian Systems; 4.1 Introduction; 4.2 cDNA Cloning and Manipulation; 4.3 Choice of Host Cell Background 4.4 Post-translational Processing of Heterologous Expressed Ion Channels4.5 Cytotoxicity; 4.6 Transient Expression Systems; 4.6.1 "Standard" Transient Expression; 4.6.2 Viral Expression Systems; 4.7 Stable Expression of Ion Channels; 4.7.1 Bicistronic Expression Systems; 4.7.2 Stable Expression of Multiple Subunits; 4.7.3 Inducible Expression; 4.8 Summary; Acknowledgements; References; 5 Analysis of Electrophysiological Data; 5.1 Overview; 5.2 Introduction; 5.3 Expression Systems and Related Recording Techniques; 5.3.1 Expression in Xenopus Oocytes; 5.3.2 Expression in Mammalian Cells 5.3.3 Leak and Capacitance Subtraction |
| Record Nr. | UNINA-9910830623203321 |
| Weinheim ; ; [Chichester], : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Expression and analysis of recombinant ion channels : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise
| Expression and analysis of recombinant ion channels : from structural studies to pharmacological screening / / edited by Jeffrey J. Clare, Derek J. Trezise |
| Pubbl/distr/stampa | Weinheim ; ; [Chichester], : Wiley-VCH, c2006 |
| Descrizione fisica | 1 online resource (305 p.) |
| Disciplina | 572.3 |
| Altri autori (Persone) |
ClareJeffrey J
TreziseDerek J |
| Soggetto topico |
Ion channels
Biological transport, Active |
| ISBN |
1-280-72342-4
9786610723423 3-527-60809-5 3-527-60793-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Expression and Analysis of Recombinant Ion Channels; Contents; Preface; List of Contributors; Color Plates; 1 Expression of Ion Channels in Xenopus Oocytes; 1.1 Introduction; 1.2 Advantages and Disadvantages of Xenopus Oocytes; 1.3 Procedures for Using Oocytes; 1.4 Types of Analyses; 1.4.1 Electrophysiological Analysis; 1.4.1.1 Two-electrode Whole Cell Voltage-clamp; 1.4.1.2 Cut-open Oocyte Voltage-clamp; 1.4.1.3 Macropatch Clamp; 1.4.1.4 Single Channel Analysis; 1.4.2 Biochemical Analysis; 1.4.3 Compound Screening; 1.4.3.1 Serial Recording Using the Roboocyte
1.4.3.2 Parallel Recording Using the OpusXpress1.5 Examples of Use; 1.5.1 Characterization of cDNA Clones for a Channel; 1.5.2 Structure-Function Correlations; 1.5.3 Studies of Human Disease Mutations; 1.6 Conclusions; Acknowledgments; References; 2 Molecular Biology Techniques for Structure - Function Studies of Ion Channels; 2.1 Introduction; 2.2 Methods for cDNA Subcloning; 2.2.1 Conventional Sub-cloning Using Restriction Enzymes and DNA Ligase; 2.2.2 PCR-based cDNA Sub-cloning; 2.2.3 Sub-cloning cDNA through Site-specific Recombination; 2.3 Generation of Chimeric Channel cDNAs 2.3.1 Use of Restriction Enzymes to Generate Chimeric Channel cDNAs2.3.2 PCR-mediated Overlap Extension for Chimera Generation; 2.3.3 PCR-mediated Integration or Replacement of cDNA Fragments; 2.4 Site-directed Mutagenesis; 2.4.1 Examples of the Use of Site-directed Mutagenesis; 2.4.2 Modification of the QuikChange Method for the Replacement of cDNA Fragments; 2.5 Epitope-tagged Channels and Fusion Partners; 2.6 Channel Subunit Concatamers; 2.7 Concluding Remarks; References; 3 Unnatural Amino Acids as Probes of Ion Channel Structure - Function and Pharmacology; 3.1 Introduction 3.2 Unnatural Amino Acid Mutagenesis Methodology3.3 Unnatural Amino Acid Mutagenesis for Ion Channel Studies; 3.4 Structure-Function Example Studies; 3.4.1 Nicotinic Acetylcholine Receptor; 3.4.2 Drug Interactions with the hERG Voltage-gated Potassium Ion Channel; 3.5 Other Uses of Unnatural Amino Acids as Probes of Protein Structure and Function; 3.6 Conclusions; Acknowledgements; References; 4 Functional Expression of Ion Channels in Mammalian Systems; 4.1 Introduction; 4.2 cDNA Cloning and Manipulation; 4.3 Choice of Host Cell Background 4.4 Post-translational Processing of Heterologous Expressed Ion Channels4.5 Cytotoxicity; 4.6 Transient Expression Systems; 4.6.1 "Standard" Transient Expression; 4.6.2 Viral Expression Systems; 4.7 Stable Expression of Ion Channels; 4.7.1 Bicistronic Expression Systems; 4.7.2 Stable Expression of Multiple Subunits; 4.7.3 Inducible Expression; 4.8 Summary; Acknowledgements; References; 5 Analysis of Electrophysiological Data; 5.1 Overview; 5.2 Introduction; 5.3 Expression Systems and Related Recording Techniques; 5.3.1 Expression in Xenopus Oocytes; 5.3.2 Expression in Mammalian Cells 5.3.3 Leak and Capacitance Subtraction |
| Record Nr. | UNINA-9910877594303321 |
| Weinheim ; ; [Chichester], : Wiley-VCH, c2006 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of ATPases [[electronic resource] ] : biochemistry, cell biology, pathophysiology / / edited by Masamitsu Futai, Yoh Wada, and Jack H. Kaplan
| Handbook of ATPases [[electronic resource] ] : biochemistry, cell biology, pathophysiology / / edited by Masamitsu Futai, Yoh Wada, and Jack H. Kaplan |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2004 |
| Descrizione fisica | 1 online resource (495 p.) |
| Disciplina |
572.3
572.475 572/.475 |
| Altri autori (Persone) |
WadaYoh
KaplanJack H |
| Soggetto topico |
Adenosine triphosphatase
Adenosine triphosphatase - Pathophysiology |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-280-52094-9
9786610520947 3-527-60612-2 3-527-60628-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Handbook of ATPases; Contents; Preface; List of Contributors; Part I P-type ATPases; 1 Yeast Plasma-membrane H(+)-ATPase: Model System for Studies of Structure, Function, Biogenesis, and Regulation; 1.1 Introduction; 1.2 Structure; 1.2.1 Ca(2+)-ATPase as a Model; 1.2.2 Applicability of the Ca(2+)-ATPase Structure to Other P(2)-ATPases, Including the Pma1 H(+)-ATPase; 1.2.3 H(+)-ATPase Oligomers; 1.2.4 Associated Proteolipids; 1.3 Reaction Mechanism; 1.3.1 Overview of the Reaction Cycle; 1.3.2 ATP Binding and Phosphorylation; 1.3.3 E1-E2 Conformational Change; 1.3.4 H(+) Pumping
1.4 Biogenesis1.4.1 Pma1 Mutants with Defects in Folding and Biogenesis; 1.4.2 Use of Pma1 Mutants to Screen for Other Genes that Play a Role in Biogenesis and Quality Control; 1.4.3 Role of Lipid Rafts; 1.5 Regulation; 1.6 Emerging Knowledge of Other Yeast P-type ATPases; Acknowledgments; References; 2 Regulation of the Sarco(endo)plasmic Reticulum Ca(2+)-ATPase by Phospholamban and Sarcolipin; 2.1 Introduction; 2.1.1 Background to Ca(2+) Signaling; 2.1.2 β-Adrenergic Signaling in the Heart; 2.2 Phospholamban-SERCA Interactions; 2.2.1 SERCA Structure and Function 2.2.2 PLN Structure and Function2.2.3 Approaches to the Study of PLN-SERCA Interactions; 2.2.4 SERCA Residues Essential for Cytoplasmic Interaction with PLN; 2.2.5 PLN Residues Essential for Cytoplasmic Interaction with SERCA; 2.2.6 PLN Residues Essential for Transmembrane Interactions with SERCA; 2.2.7 SERCA Residues Essential for Transmembrane Interactions with PLN; 2.2.8 Structural Modeling of the PLN-SERCA Inhibitory Interaction; 2.3 Physiological Role of PLN in Basal Cardiac Function; 2.3.1 Alterations in PLN Levels and Function by Transcription and Phosphorylation 2.3.2 Targeting of PLN2.3.3 Role of PLN in Smooth and Skeletal Muscles; 2.3.4 Overexpression of PLN; 2.3.5 Physiological Role of PLN in β-Adrenergic Stimulation; 2.3.6 Superinhibitory PLN Mutants; 2.4 Phospholamban in Heart Failure; 2.4.1 Introduction; 2.4.2 Potential Therapies; 2.5 Human PLN Mutations as a Cause of Cardiomyopathy; 2.5.1 PLN R9C Mutant; 2.5.2 PLN L39stop Mutant; 2.6 Sarcolipin; 2.6.1 Introduction; 2.7 Physiological Role of SLN; 2.7.1 SLN Expression; 2.7.2 Overexpression of SLN; 2.7.2.1 Response of the SLN Gene to Chronic Stimulation 2.7.3 Inhibition of SERCA Function by SLN Plus PLN2.7.4 Modeling of the SLN-SERCA and SLN-PLN-SERCA Interactions; Acknowledgments; References; 3 Catalytic and Transport Mechanism of the Sarco-(Endo)Plasmic Reticulum Ca(2+)-ATPase (SERCA); Summary; 3.1 Introduction; 3.2 Experimental Systems; 3.3 Functional Characterization; 3.4 Structural Characterization; 3.4.1 Extramembranous Region and the Catalytic Domains of E1·2Ca(2+); 3.4.2 Transmembrane region of E1·2Ca(2+); 3.4.3 Enzyme Structure in the Absence of Ca(2+) (E2·TG); 3.4.4 Thapsigargin-binding Domain; 3.4.5 Interaction with Phospholamban 3.5 Binding of Ligands, Catalytic Events and Conformational Changes |
| Record Nr. | UNINA-9910143964803321 |
| Weinheim, : Wiley-VCH, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of ATPases [[electronic resource] ] : biochemistry, cell biology, pathophysiology / / edited by Masamitsu Futai, Yoh Wada, and Jack H. Kaplan
| Handbook of ATPases [[electronic resource] ] : biochemistry, cell biology, pathophysiology / / edited by Masamitsu Futai, Yoh Wada, and Jack H. Kaplan |
| Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2004 |
| Descrizione fisica | 1 online resource (495 p.) |
| Disciplina |
572.3
572.475 572/.475 |
| Altri autori (Persone) |
WadaYoh
KaplanJack H |
| Soggetto topico |
Adenosine triphosphatase
Adenosine triphosphatase - Pathophysiology |
| ISBN |
1-280-52094-9
9786610520947 3-527-60612-2 3-527-60628-9 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Handbook of ATPases; Contents; Preface; List of Contributors; Part I P-type ATPases; 1 Yeast Plasma-membrane H(+)-ATPase: Model System for Studies of Structure, Function, Biogenesis, and Regulation; 1.1 Introduction; 1.2 Structure; 1.2.1 Ca(2+)-ATPase as a Model; 1.2.2 Applicability of the Ca(2+)-ATPase Structure to Other P(2)-ATPases, Including the Pma1 H(+)-ATPase; 1.2.3 H(+)-ATPase Oligomers; 1.2.4 Associated Proteolipids; 1.3 Reaction Mechanism; 1.3.1 Overview of the Reaction Cycle; 1.3.2 ATP Binding and Phosphorylation; 1.3.3 E1-E2 Conformational Change; 1.3.4 H(+) Pumping
1.4 Biogenesis1.4.1 Pma1 Mutants with Defects in Folding and Biogenesis; 1.4.2 Use of Pma1 Mutants to Screen for Other Genes that Play a Role in Biogenesis and Quality Control; 1.4.3 Role of Lipid Rafts; 1.5 Regulation; 1.6 Emerging Knowledge of Other Yeast P-type ATPases; Acknowledgments; References; 2 Regulation of the Sarco(endo)plasmic Reticulum Ca(2+)-ATPase by Phospholamban and Sarcolipin; 2.1 Introduction; 2.1.1 Background to Ca(2+) Signaling; 2.1.2 β-Adrenergic Signaling in the Heart; 2.2 Phospholamban-SERCA Interactions; 2.2.1 SERCA Structure and Function 2.2.2 PLN Structure and Function2.2.3 Approaches to the Study of PLN-SERCA Interactions; 2.2.4 SERCA Residues Essential for Cytoplasmic Interaction with PLN; 2.2.5 PLN Residues Essential for Cytoplasmic Interaction with SERCA; 2.2.6 PLN Residues Essential for Transmembrane Interactions with SERCA; 2.2.7 SERCA Residues Essential for Transmembrane Interactions with PLN; 2.2.8 Structural Modeling of the PLN-SERCA Inhibitory Interaction; 2.3 Physiological Role of PLN in Basal Cardiac Function; 2.3.1 Alterations in PLN Levels and Function by Transcription and Phosphorylation 2.3.2 Targeting of PLN2.3.3 Role of PLN in Smooth and Skeletal Muscles; 2.3.4 Overexpression of PLN; 2.3.5 Physiological Role of PLN in β-Adrenergic Stimulation; 2.3.6 Superinhibitory PLN Mutants; 2.4 Phospholamban in Heart Failure; 2.4.1 Introduction; 2.4.2 Potential Therapies; 2.5 Human PLN Mutations as a Cause of Cardiomyopathy; 2.5.1 PLN R9C Mutant; 2.5.2 PLN L39stop Mutant; 2.6 Sarcolipin; 2.6.1 Introduction; 2.7 Physiological Role of SLN; 2.7.1 SLN Expression; 2.7.2 Overexpression of SLN; 2.7.2.1 Response of the SLN Gene to Chronic Stimulation 2.7.3 Inhibition of SERCA Function by SLN Plus PLN2.7.4 Modeling of the SLN-SERCA and SLN-PLN-SERCA Interactions; Acknowledgments; References; 3 Catalytic and Transport Mechanism of the Sarco-(Endo)Plasmic Reticulum Ca(2+)-ATPase (SERCA); Summary; 3.1 Introduction; 3.2 Experimental Systems; 3.3 Functional Characterization; 3.4 Structural Characterization; 3.4.1 Extramembranous Region and the Catalytic Domains of E1·2Ca(2+); 3.4.2 Transmembrane region of E1·2Ca(2+); 3.4.3 Enzyme Structure in the Absence of Ca(2+) (E2·TG); 3.4.4 Thapsigargin-binding Domain; 3.4.5 Interaction with Phospholamban 3.5 Binding of Ligands, Catalytic Events and Conformational Changes |
| Record Nr. | UNINA-9910830901403321 |
| Weinheim, : Wiley-VCH, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Handbook of biopolymer-based materials : from blends and composites to gels and complex networks / / S. Thomas ...[et.al.]
| Handbook of biopolymer-based materials : from blends and composites to gels and complex networks / / S. Thomas ...[et.al.] |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Weinheim, : Wiley, 2013 |
| Descrizione fisica | 1 online resource (909 p.) |
| Disciplina |
572.3
572.33 |
| Altri autori (Persone) | ThomasSabu |
| Soggetto topico |
Biopolymers
Biotechnology |
| ISBN |
3-527-65247-7
3-527-65245-0 1-299-46438-6 3-527-65248-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Handbook of Biopolymer-Based Materials: From Blends and Composites to Gels and Complex Networks; Contents; Foreword; List of Contributors; 1 Biopolymers: State of the Art, New Challenges, and Opportunities; 1.1 Introduction; 1.2 Biopolymers: A Niche For Fundamental Research in Soft Matter Physics; 1.3 Biopolymers: An Endless Source of Applications; 1.4 Topics Covered by the Book; 1.5 Conclusions; References; 2 General Overview of Biopolymers: Structure, Properties, and Applications; 2.1 Introduction; 2.2 Plant Cell Wall Polysaccharides; 2.2.1 Cellulose; 2.2.1.1 Cellulose Extraction
2.2.1.2 Nanocellulose2.2.1.3 Microfibrillated Cellulose; 2.2.1.4 Cellulose Nanowhiskers; 2.2.2 Hemicelluloses; 2.2.2.1 Galactomannans; 2.2.2.2 Konjac Glucomannan; 2.2.2.3 Xylan; 2.2.2.4 Xyloglucan; 2.2.3 Pectins; 2.3 Biocomposites; 2.3.1 Natural Fiber Composites; 2.3.2 Cellulose Composites; 2.3.3 Cellulose-Polymer Interactions; 2.3.4 Semi-Solid Composites; 2.4 Future Outlook; References; 3 Biopolymers from Plants; 3.1 Introduction; 3.2 Lipid and Phenolic Biopolymers; 3.2.1 The Biopolymer Cutin; 3.2.1.1 Cutin Monomers: Biosynthesis and Physicochemical Characteristics 3.2.1.2 Molecular Architecture of Cutin3.2.1.3 Cutin Biosynthesis; 3.2.2 Lignin; 3.2.2.1 Monomer Precursors and Chemical Reactivity; 3.2.2.2 Lignin Biosynthesis; 3.2.3 Suberin; 3.2.3.1 Chemical Composition; 3.2.3.2 Biosynthesis and Fine Structure; 3.3 Carbohydrate Biopolymers: Polysaccharides; 3.3.1 Structural Polysaccharides; 3.3.1.1 Cellulose; 3.3.1.2 Hemicellulose; 3.3.1.3 Pectin; 3.3.2 Storage Polysaccharides; 3.3.2.1 Starch; 3.3.2.2 Fructans: Inulin; 3.3.3 Other: Gums (Guar Gum, Gum Arabic, Gum Karaya, Gum Tragacanth, and Locust Bean Gum); 3.4 Isoprene Biopolymers: Natural Rubber 3.4.1 cis-Polyisoprene3.4.1.1 Occurrence; 3.4.1.2 Composition, Structure, and Properties; 3.4.1.3 cis-1,4-Polyisoprene Biosynthesis; 3.4.1.4 Applications; 3.4.2 trans-Polyisoprene; 3.5 Concluding Remarks; References; 4 Bacterial Biopolymers and Genetically Engineered Biopolymers for Gel Systems Application; 4.1 Introduction; 4.1.1 Nucleic Acid Biopolymers: Central Dogma; 4.2 Microbial Polysaccharides as Biopolymers; 4.2.1 Synthesis and Applications; 4.3 Microbial Biopolymers as Drug Delivery Vehicle; 4.3.1 ε-Poly-L-Lysine (ε-PL) and Its Applications 4.3.2 Polyhydroxyalkanoates and Its Applications4.4 Polyanhydrides; 4.5 Recombinant Protein Polymer Production; 4.6 Recombinant Genetically Engineered Biopolymer : Elastin; 4.7 Collagen as an Ideal Biopolymer; 4.7.1 Microbial Recombinant Collagens: Production in Pichia Pastoris; 4.8 Biopolymers for Gel System; 4.9 Hydrogels of Biopolymers for Regenerative Medicine; 4.9.1 Polysaccharide Hydrogels; 4.9.2 Cellulose-Derived Biopolymers-Based Hydrogels; 4.9.3 Protein Biopolymers-Based Hydrogels; 4.10 Supermacroporous Cryogel Matrix from Biopolymers; 4.10.1 Protein Cryogel 4.11 Biopolymers Impact on Environment |
| Record Nr. | UNINA-9910139007803321 |
| Weinheim, : Wiley, 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Immobilized microbial cells : based on a symposium jointly sponsored by the ACS Divisions of Microbial and Biochemical Technology, Agricultural and food Chemistry and carbohydrate Chemistry at the 176th meeting of the American Chemical Society, Miami Beach, Florida, September 14, 1978 / K. Venkatsubramanian
| Immobilized microbial cells : based on a symposium jointly sponsored by the ACS Divisions of Microbial and Biochemical Technology, Agricultural and food Chemistry and carbohydrate Chemistry at the 176th meeting of the American Chemical Society, Miami Beach, Florida, September 14, 1978 / K. Venkatsubramanian |
| Autore | Venkatsubramanian, K. |
| Pubbl/distr/stampa | Washington : American Chemical Society, 1979 |
| Descrizione fisica | X, 257 p. ; 24 cm |
| Disciplina | 572.3 |
| Soggetto non controllato | Biochimica - Cellule microbiche |
| ISBN | 0-8412-0508-6 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910319246903321 |
Venkatsubramanian, K.
|
||
| Washington : American Chemical Society, 1979 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Ion channels of excitable membranes / Bertil Hille
| Ion channels of excitable membranes / Bertil Hille |
| Autore | Hille, Bertil <1940- > |
| Edizione | [3. ed] |
| Pubbl/distr/stampa | Sunderland (MA), : Sinauer, c2001 |
| Descrizione fisica | XVIII, 814 p., [4] c. di tav. : ill. ; 24 cm. |
| Disciplina |
572
572.3 |
| Soggetto topico |
Membrana cellulare
Cellule muscolari Neuroni |
| ISBN | 0878933212 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNISANNIO-NAP0431915 |
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Hille, Bertil <1940- >
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| Sunderland (MA), : Sinauer, c2001 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. del Sannio | ||
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Ion exchange membranes [[electronic resource] ] : preparation, characterization, modification and application / / Toshikatsu Sata
| Ion exchange membranes [[electronic resource] ] : preparation, characterization, modification and application / / Toshikatsu Sata |
| Autore | Sata Toshikatsu |
| Pubbl/distr/stampa | Cambridge, : Royal Society of Chemistry, c2004 |
| Descrizione fisica | 1 online resource (325 p.) |
| Disciplina | 572.3 |
| Soggetto topico | Ion-permeable membranes |
| Soggetto genere / forma | Electronic books. |
| ISBN | 1-84755-117-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
IEM-PRE; IEM-1; 1.1&X; Background; Table 1; 1.2&X; References; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; mkr29; mkr30; IEM-2; 2.1&X; Introduction; 2.2&X; Flux Equation; Equation 3; Equation 4; Equation 5; Equation 6; Equation 6; Equation 7; Equation 9; Equation 10; Equation 11; Equation 12; Permselectivity of Ions Through the Ion Exchange Membrane; Equation 13; Equation 14; Equation 15; Equation 16; Equation 17; Equation 18; Equation 19
Equation 20 Equation 21; Equation 22; Equation 23; Equation 24; Equation 25; Equation 26; Equation 27; Equation 28; Equation 29; Equation 30; Equation 31; Equation 32; Equation 33; Equation 34; Equation 35; Membrane Potential; Figure 1; Equation 36; Equation 39; Equation 40; Equation 41; Equation 43; Equation 44; Figure 2; Equation 49; Equation 50; Bionic Potential; Equation 51; Equation 52; Equation 53; Equation 54; Electrical Conductivity of Ion Exchange Membrane; Equation 56; Equation 57; Equation 58; Diffusion of Electrolyte Through Ion Exchange Membranes Equation 57 Equation 58; Equation 59; Equation 60; Equation 61; Equation 62; Equation 63; Equation 66; Equation 68; Equation 69; Equation 70; Equation 71; Diffusion of Non-Electrolyte Through Ion Exchange Membranes; Equation 72;Self-diffusion Through Ion Exchange Membranes; Equation 74; Equation 75; Equation 76; Equation 77; Equation 78; Figure 3; Figure 4; Osmosis; Equation 79; Electro-osmosis; Figure 5; Equation 80; Equation 83; Equation 84; Equation 85; 2.12&X; Hydrodynamic Permeability of Solvent; Figure 6; Equation 86; Equation 87; Equation 88; Equation 89 Equation 90 Equation 93; Equation 94; Equation 95; Equation 96; Equation 97; Equation 98; Equation 99; Permselectivity of Ions with the Same Charge; Equation 8; Figure 7; Equation 101; Equation 102; Equation 105; Equation 106; Conclusions; References; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; IEM-3; 3.1&X; Introduction; 3.2&X; Classification of Ion Exchange Membranes; Table 1; 3.3&X General Explanation of Preparation Methods of Ion Exchange Membranes 3.3.1&Y; Heterogeneous Ion Exchange Membranes; 3.3.2&Y; Homogeneous Ion Exchange Membranes&Y; ; 3.3.2.1&Z; Ion Exchange Membranes Prepared by Condensation Reaction of Ionic Monomeric Com-pounds; Figure 1; 3.3.2.2&Z; Ion Exchange Membranes Prepared by Polymerization of Vinyl Monomers; Preparation of polymer block and slicing the block into films.&D-end; After styrene has been partially polymerized by heating, d; Figure 2; Table 2; Polymerization of vinyl monomers into films (coating method or paste method).&D-end1 Here, linear polymers without ion exchange |
| Record Nr. | UNINA-9910454332703321 |
|
Sata Toshikatsu
|
||
| Cambridge, : Royal Society of Chemistry, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Ion exchange membranes [[electronic resource] ] : preparation, characterization, modification and application / / Toshikatsu Sata
| Ion exchange membranes [[electronic resource] ] : preparation, characterization, modification and application / / Toshikatsu Sata |
| Autore | Sata Toshikatsu |
| Pubbl/distr/stampa | Cambridge, : Royal Society of Chemistry, c2004 |
| Descrizione fisica | 1 online resource (325 p.) |
| Disciplina | 572.3 |
| Soggetto topico | Ion-permeable membranes |
| ISBN | 1-84755-117-3 |
| Classificazione | 51.99 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
IEM-PRE; IEM-1; 1.1&X; Background; Table 1; 1.2&X; References; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; mkr27; mkr28; mkr29; mkr30; IEM-2; 2.1&X; Introduction; 2.2&X; Flux Equation; Equation 3; Equation 4; Equation 5; Equation 6; Equation 6; Equation 7; Equation 9; Equation 10; Equation 11; Equation 12; Permselectivity of Ions Through the Ion Exchange Membrane; Equation 13; Equation 14; Equation 15; Equation 16; Equation 17; Equation 18; Equation 19
Equation 20 Equation 21; Equation 22; Equation 23; Equation 24; Equation 25; Equation 26; Equation 27; Equation 28; Equation 29; Equation 30; Equation 31; Equation 32; Equation 33; Equation 34; Equation 35; Membrane Potential; Figure 1; Equation 36; Equation 39; Equation 40; Equation 41; Equation 43; Equation 44; Figure 2; Equation 49; Equation 50; Bionic Potential; Equation 51; Equation 52; Equation 53; Equation 54; Electrical Conductivity of Ion Exchange Membrane; Equation 56; Equation 57; Equation 58; Diffusion of Electrolyte Through Ion Exchange Membranes Equation 57 Equation 58; Equation 59; Equation 60; Equation 61; Equation 62; Equation 63; Equation 66; Equation 68; Equation 69; Equation 70; Equation 71; Diffusion of Non-Electrolyte Through Ion Exchange Membranes; Equation 72;Self-diffusion Through Ion Exchange Membranes; Equation 74; Equation 75; Equation 76; Equation 77; Equation 78; Figure 3; Figure 4; Osmosis; Equation 79; Electro-osmosis; Figure 5; Equation 80; Equation 83; Equation 84; Equation 85; 2.12&X; Hydrodynamic Permeability of Solvent; Figure 6; Equation 86; Equation 87; Equation 88; Equation 89 Equation 90 Equation 93; Equation 94; Equation 95; Equation 96; Equation 97; Equation 98; Equation 99; Permselectivity of Ions with the Same Charge; Equation 8; Figure 7; Equation 101; Equation 102; Equation 105; Equation 106; Conclusions; References; mkr1; mkr2; mkr3; mkr4; mkr5; mkr6; mkr7; mkr8; mkr9; mkr10; mkr11; mkr12; mkr13; mkr14; mkr15; mkr16; mkr17; mkr18; mkr19; mkr20; mkr21; mkr22; mkr23; mkr24; mkr25; mkr26; IEM-3; 3.1&X; Introduction; 3.2&X; Classification of Ion Exchange Membranes; Table 1; 3.3&X General Explanation of Preparation Methods of Ion Exchange Membranes 3.3.1&Y; Heterogeneous Ion Exchange Membranes; 3.3.2&Y; Homogeneous Ion Exchange Membranes&Y; ; 3.3.2.1&Z; Ion Exchange Membranes Prepared by Condensation Reaction of Ionic Monomeric Com-pounds; Figure 1; 3.3.2.2&Z; Ion Exchange Membranes Prepared by Polymerization of Vinyl Monomers; Preparation of polymer block and slicing the block into films.&D-end; After styrene has been partially polymerized by heating, d; Figure 2; Table 2; Polymerization of vinyl monomers into films (coating method or paste method).&D-end1 Here, linear polymers without ion exchange |
| Record Nr. | UNINA-9910782759703321 |
|
Sata Toshikatsu
|
||
| Cambridge, : Royal Society of Chemistry, c2004 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
