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Molecular Fluorescence: Principles and Applications
| Molecular Fluorescence: Principles and Applications |
| Autore | Valeur Bernard |
| Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH Imprint, 2002 |
| Descrizione fisica | 1 online resource (399 pages) |
| Disciplina | 543/.08584 |
| Soggetto topico |
Fluorescence spectroscopy
Analytical Chemistry Chemistry Physical Sciences & Mathematics |
| ISBN |
1-280-55768-0
9786610557684 3-527-60024-8 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910829871203321 |
Valeur Bernard
|
||
| [Place of publication not identified], : Wiley VCH Imprint, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular Fluorescence: Principles and Applications
| Molecular Fluorescence: Principles and Applications |
| Autore | Valeur Bernard |
| Pubbl/distr/stampa | [Place of publication not identified], : Wiley VCH Imprint, 2002 |
| Descrizione fisica | 1 online resource (399 pages) |
| Disciplina | 543/.08584 |
| Soggetto topico |
Fluorescence spectroscopy
Analytical Chemistry Chemistry Physical Sciences & Mathematics |
| ISBN |
1-280-55768-0
9786610557684 3-527-60024-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNINA-9910840590703321 |
|
Valeur Bernard
|
||
| [Place of publication not identified], : Wiley VCH Imprint, 2002 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular fluorescent sensors for cellular studies / / edited by Elizabeth J. New
| Molecular fluorescent sensors for cellular studies / / edited by Elizabeth J. New |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, Incorporated, , 2022 |
| Descrizione fisica | 1 online resource (307 pages) |
| Soggetto topico |
Fluorescent probes
Biosensors Fluorescence spectroscopy |
| ISBN |
9781119749844
1-119-74984-0 1-119-74980-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright Page -- Contents -- List of Contributors -- Chapter 1 An Introduction to Small Molecule Fluorescent Sensors -- 1.1 What is Fluorescence? -- 1.2 Why Is Fluorescence Useful? -- 1.3 What Is a Fluorescent Sensor? -- 1.4 General Types of Fluorescent Sensors -- 1.5 Important Parameters -- 1.5.1 Excitation Maxima -- 1.5.2 Emission Maxima -- 1.5.3 Stokes Shift -- 1.5.4 Quantum Yield -- 1.5.5 Molar Extinction Coefficient -- 1.5.6 Brightness -- 1.5.7 Lifetime -- 1.5.8 Photobleaching -- 1.5.9 Anisotropy -- 1.5.10 Quenching -- 1.6 Fluorescence Mechanisms Used in Fluorescent Sensors -- 1.6.1 Photoinduced Electron Transfer -- 1.6.2 Internal Charge Transfer -- 1.6.3 Förster Resonance Energy Transfer -- 1.6.4 Through Bond Energy Transfer -- 1.6.5 Excited-State Intramolecular Proton Transfer -- 1.6.6 Aggregation-Induced Emission -- 1.6.7 Excimer Formation -- 1.7 Commonly Used Fluorophores -- 1.7.1 Fluorescein -- 1.7.2 Rhodamine -- 1.7.3 Coumarin -- 1.7.4 Naphthalimide -- 1.7.5 BODIPY (4,4-Difluoro4-bora-3a,4a-diaza-s-indacene) -- 1.7.6 Cyanine -- 1.8 Summary -- References -- Chapter 2 The Applications of Responsive Fluorescent Sensors to Biological Systems -- 2.1 Criteria for Biologically Relevant Fluorescent Sensors -- 2.2 Microscopy for Visualising Fluorescent Sensors -- 2.2.1 Important Considerations in Microscopy -- 2.2.2 Common Microscopy Techniques -- 2.3 Other Instrumental Techniques for Studying Cells Treated with Fluorescent Sensors -- 2.3.1 Flow Cytometry -- 2.3.2 Fluorescence Plate-readers -- 2.4 Biological Samples to Which Fluorescent Sensors Can Be Applied -- 2.4.1 Cultured Mammalian Cells -- 2.4.2 Bacteria -- 2.4.3 Plants -- 2.4.4 Multi-cellular Organisms -- 2.4.5 Towards In Vivo Imaging -- 2.5 Common Challenges and Misconceptions in the Applications of Fluorescent Sensors.
2.5.1 Important Considerations in Applying Sensors -- 2.5.2 Common Misconceptions About the Use of Sensors - The Bridge Between Multiple Disciplines -- 2.6 Conclusions -- References -- Chapter 3 Methods to Control the Subcellular Localisation of Fluorescent Sensors -- 3.1 Introduction -- 3.2 Targeting the Nucleus -- 3.3 Targeting Mitochondria -- 3.4 Targeting Lysosomes -- 3.5 Targeting Endosomes -- 3.6 Targeting Autophagic Compartments -- 3.7 Targeting Peroxisomes -- 3.8 Targeting the Endoplasmic Reticulum -- 3.9 Targeting the Golgi Apparatus -- 3.10 Targeting Lipid Droplets -- 3.11 Targeting the Plasma Membrane -- 3.12 Targeting the Cytoskeleton -- 3.13 Targeting the Cytosol -- 3.14 Trapping and Accumulation of Sensors -- References -- Chapter 4 Recognition-based Sensors for Cellular Imaging -- 4.1 Considerations for Recognition-based Sensing -- 4.1.1 Receptor-Analyte Recognition and Binding Affinity -- 4.1.2 Key Considerations to Enhance Selective Receptor to Analyte Recognition -- 4.2 Recognition-based Cation Sensing -- 4.2.1 Group I and II Metal Sensing -- 4.2.2 Essential Transition Metal Sensing -- 4.2.3 Toxic Metal Sensing -- 4.3 Recognition-based Anion Sensing -- 4.3.1 Anion Sensing Approaches -- 4.3.2 Halogen Ions Sensing -- 4.3.3 Inorganic Phosphates and Pyrophosphates -- 4.3.4 Bicarbonate, Hydrogen Sulfate, and Nitrate -- 4.4 Conclusions -- References -- Chapter 5 Activity-based Fluorescent Sensors and Their Applications in Biological Studies -- 5.1 Introduction -- 5.1.1 Design Principles -- 5.2 Oxidation Reactions for Sensing Oxidative Species -- 5.2.1 Fluorescent Sensors for Hydrogen Peroxide -- 5.2.2 Fluorescent Sensors for Peroxynitrite -- 5.2.3 Fluorescent Sensors for Hypochlorous Acid -- 5.2.4 Fluorescent Sensors for Nitric Oxide -- 5.2.5 Fluorescent Sensors for Singlet Oxygen -- 5.3 Reduction Reactions for Sensing Reductive Species. 5.3.1 Fluorescent Sensors for Hydrogen Sulfides -- 5.3.2 Fluorescent Sensors for Glutathione, Cysteine, and Homocysteine -- 5.3.3 Fluorescent Sensors for Selenocysteine -- 5.4 Reactions for Sensing Carbonyl Species -- 5.4.1 Fluorescent Sensors for Formaldehyde -- 5.4.2 Fluorescent Sensors for Methylglyoxal -- 5.5 Metal-mediated Reactions -- 5.6 Metal-sensing Reactions -- 5.7 Enzymatic Reactions -- 5.8 Reversible Reactions -- 5.8.1 Nucleophilic Conjugate Additions -- 5.8.2 Nucleophilic Addition -- 5.8.3 Imine Formation -- 5.8.4 Oxidation-Reduction Reactions -- 5.9 Analyte Regeneration -- 5.10 Summary -- References -- Chapter 6 Fluorescent Sensors of the Cellular Environment -- 6.1 Fluorescent Sensors for Polarity and Viscosity -- 6.1.1 The Biological Significance of Polarity and Viscosity -- 6.1.2 Twisted Intramolecular Charge Transfer as a Mechanism for Polarity and Viscosity Sensing -- 6.1.3 Polarity Sensors Based on Other Mechanisms -- 6.2 Fluorescent Sensors for pH -- 6.2.1 The Regulation of pH in Health and Disease -- 6.2.2 Considerations and Design Strategies for the Preparation of pH Sensors -- 6.2.3 Examples of pH Sensors -- 6.3 Fluorescent Redox Sensors for Biological Studies -- 6.3.1 The Regulation of Redox State in Health and Disease -- 6.3.2 Design Strategies of Fluorescent Redox Sensors and Key Examples -- 6.4 Conclusions -- References -- Chapter 7 Labelling Proteins and Biomolecules with Small Fluorescent Sensors -- 7.1 Labelling Biomolecules in Cells with Fluorescent Sensors -- 7.2 Small-molecule Modifications and Bioorthogonal Reactions -- 7.2.1 Polar Ketone and Aldehyde Condensations -- 7.2.2 Azide Bioorthogonal Chemistry -- 7.2.3 Tetrazine Ligation -- 7.2.4 Commercial Fluorescent Labels -- 7.3 Short peptide Recognition Sequences -- 7.4 Fusion Protein Tagging Systems -- 7.4.1 FKBP Tag -- 7.4.2 eDHFR Tag -- 7.4.3 PYP Tag. 7.4.4 SNAP-Tag and CLIP-Tag -- 7.4.5 HaloTag -- 7.5 Enzymatic Modifications for Labelling Proteins -- 7.5.1 The LAP-tag System -- 7.5.2 Protein Trans-splicing -- 7.6 Future Developments -- References -- Chapter 8 Future Directions of Fluorescence Sensors for Cellular Studies -- 8.1 Fluorescence Lifetime Imaging Microscopy -- 8.1.1 Introduction -- 8.1.2 Advantages of Fluorescence Lifetime Imaging Microscopy -- 8.1.3 Examples of Sensors for FLIM -- 8.1.4 Future Directions -- 8.2 Near-infrared Sensors -- 8.2.1 Strategies to Make NIR Sensors -- 8.2.2 NIR Fluorophore Scaffolds -- 8.2.3 Future Directions -- 8.3 Dual-analyte Sensing -- 8.3.1 Introduction -- 8.3.2 Recognition-Based Dual-analyte Sensors -- 8.3.3 Activity-based Dual-analyte Sensors -- 8.3.4 Mixed Dual-analyte Sensors -- 8.3.5 Sequence-specific Reactions -- 8.3.6 Conclusions and Future Directions -- 8.4 Super-resolution Microscopy -- 8.4.1 Introduction -- 8.4.2 Super-resolution Microscopy Techniques -- 8.4.3 Considerations for Use of Super Resolution Microscopy -- 8.4.4 Fluorescent Sensors for Super-resolution Microscopy -- 8.4.5 Future Directions -- 8.5 Multimodality -- 8.5.1 Introduction -- 8.5.2 Radioisotope Techniques -- 8.5.3 Computed Tomography -- 8.5.4 Magnetic Resonance Imaging -- 8.5.5 Photoacoustic Imaging -- 8.5.6 Vibrational Spectroscopy -- 8.5.7 Synchrotron X-ray Techniques -- 8.5.8 Mass Spectrometry -- 8.5.9 Electron Microscopy -- 8.5.10 Three or More Modalities -- 8.5.11 Future Directions -- References -- Index -- EULA. |
| Record Nr. | UNINA-9910590101003321 |
| Chichester, West Sussex : , : John Wiley & Sons, Incorporated, , 2022 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular fluorescent sensors for cellular studies / / edited by Elizabeth J. New
| Molecular fluorescent sensors for cellular studies / / edited by Elizabeth J. New |
| Pubbl/distr/stampa | Chichester, West Sussex, England ; ; Oxford, England : , : Wiley, , [2022] |
| Descrizione fisica | 1 online resource (307 pages) |
| Disciplina | 610.28 |
| Soggetto topico |
Biosensors
Fluorescence spectroscopy |
| ISBN |
9781119749844
1-119-74984-0 1-119-74980-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Title Page -- Copyright Page -- Contents -- List of Contributors -- Chapter 1 An Introduction to Small Molecule Fluorescent Sensors -- 1.1 What is Fluorescence? -- 1.2 Why Is Fluorescence Useful? -- 1.3 What Is a Fluorescent Sensor? -- 1.4 General Types of Fluorescent Sensors -- 1.5 Important Parameters -- 1.5.1 Excitation Maxima -- 1.5.2 Emission Maxima -- 1.5.3 Stokes Shift -- 1.5.4 Quantum Yield -- 1.5.5 Molar Extinction Coefficient -- 1.5.6 Brightness -- 1.5.7 Lifetime -- 1.5.8 Photobleaching -- 1.5.9 Anisotropy -- 1.5.10 Quenching -- 1.6 Fluorescence Mechanisms Used in Fluorescent Sensors -- 1.6.1 Photoinduced Electron Transfer -- 1.6.2 Internal Charge Transfer -- 1.6.3 Förster Resonance Energy Transfer -- 1.6.4 Through Bond Energy Transfer -- 1.6.5 Excited-State Intramolecular Proton Transfer -- 1.6.6 Aggregation-Induced Emission -- 1.6.7 Excimer Formation -- 1.7 Commonly Used Fluorophores -- 1.7.1 Fluorescein -- 1.7.2 Rhodamine -- 1.7.3 Coumarin -- 1.7.4 Naphthalimide -- 1.7.5 BODIPY (4,4-Difluoro4-bora-3a,4a-diaza-s-indacene) -- 1.7.6 Cyanine -- 1.8 Summary -- References -- Chapter 2 The Applications of Responsive Fluorescent Sensors to Biological Systems -- 2.1 Criteria for Biologically Relevant Fluorescent Sensors -- 2.2 Microscopy for Visualising Fluorescent Sensors -- 2.2.1 Important Considerations in Microscopy -- 2.2.2 Common Microscopy Techniques -- 2.3 Other Instrumental Techniques for Studying Cells Treated with Fluorescent Sensors -- 2.3.1 Flow Cytometry -- 2.3.2 Fluorescence Plate-readers -- 2.4 Biological Samples to Which Fluorescent Sensors Can Be Applied -- 2.4.1 Cultured Mammalian Cells -- 2.4.2 Bacteria -- 2.4.3 Plants -- 2.4.4 Multi-cellular Organisms -- 2.4.5 Towards In Vivo Imaging -- 2.5 Common Challenges and Misconceptions in the Applications of Fluorescent Sensors.
2.5.1 Important Considerations in Applying Sensors -- 2.5.2 Common Misconceptions About the Use of Sensors - The Bridge Between Multiple Disciplines -- 2.6 Conclusions -- References -- Chapter 3 Methods to Control the Subcellular Localisation of Fluorescent Sensors -- 3.1 Introduction -- 3.2 Targeting the Nucleus -- 3.3 Targeting Mitochondria -- 3.4 Targeting Lysosomes -- 3.5 Targeting Endosomes -- 3.6 Targeting Autophagic Compartments -- 3.7 Targeting Peroxisomes -- 3.8 Targeting the Endoplasmic Reticulum -- 3.9 Targeting the Golgi Apparatus -- 3.10 Targeting Lipid Droplets -- 3.11 Targeting the Plasma Membrane -- 3.12 Targeting the Cytoskeleton -- 3.13 Targeting the Cytosol -- 3.14 Trapping and Accumulation of Sensors -- References -- Chapter 4 Recognition-based Sensors for Cellular Imaging -- 4.1 Considerations for Recognition-based Sensing -- 4.1.1 Receptor-Analyte Recognition and Binding Affinity -- 4.1.2 Key Considerations to Enhance Selective Receptor to Analyte Recognition -- 4.2 Recognition-based Cation Sensing -- 4.2.1 Group I and II Metal Sensing -- 4.2.2 Essential Transition Metal Sensing -- 4.2.3 Toxic Metal Sensing -- 4.3 Recognition-based Anion Sensing -- 4.3.1 Anion Sensing Approaches -- 4.3.2 Halogen Ions Sensing -- 4.3.3 Inorganic Phosphates and Pyrophosphates -- 4.3.4 Bicarbonate, Hydrogen Sulfate, and Nitrate -- 4.4 Conclusions -- References -- Chapter 5 Activity-based Fluorescent Sensors and Their Applications in Biological Studies -- 5.1 Introduction -- 5.1.1 Design Principles -- 5.2 Oxidation Reactions for Sensing Oxidative Species -- 5.2.1 Fluorescent Sensors for Hydrogen Peroxide -- 5.2.2 Fluorescent Sensors for Peroxynitrite -- 5.2.3 Fluorescent Sensors for Hypochlorous Acid -- 5.2.4 Fluorescent Sensors for Nitric Oxide -- 5.2.5 Fluorescent Sensors for Singlet Oxygen -- 5.3 Reduction Reactions for Sensing Reductive Species. 5.3.1 Fluorescent Sensors for Hydrogen Sulfides -- 5.3.2 Fluorescent Sensors for Glutathione, Cysteine, and Homocysteine -- 5.3.3 Fluorescent Sensors for Selenocysteine -- 5.4 Reactions for Sensing Carbonyl Species -- 5.4.1 Fluorescent Sensors for Formaldehyde -- 5.4.2 Fluorescent Sensors for Methylglyoxal -- 5.5 Metal-mediated Reactions -- 5.6 Metal-sensing Reactions -- 5.7 Enzymatic Reactions -- 5.8 Reversible Reactions -- 5.8.1 Nucleophilic Conjugate Additions -- 5.8.2 Nucleophilic Addition -- 5.8.3 Imine Formation -- 5.8.4 Oxidation-Reduction Reactions -- 5.9 Analyte Regeneration -- 5.10 Summary -- References -- Chapter 6 Fluorescent Sensors of the Cellular Environment -- 6.1 Fluorescent Sensors for Polarity and Viscosity -- 6.1.1 The Biological Significance of Polarity and Viscosity -- 6.1.2 Twisted Intramolecular Charge Transfer as a Mechanism for Polarity and Viscosity Sensing -- 6.1.3 Polarity Sensors Based on Other Mechanisms -- 6.2 Fluorescent Sensors for pH -- 6.2.1 The Regulation of pH in Health and Disease -- 6.2.2 Considerations and Design Strategies for the Preparation of pH Sensors -- 6.2.3 Examples of pH Sensors -- 6.3 Fluorescent Redox Sensors for Biological Studies -- 6.3.1 The Regulation of Redox State in Health and Disease -- 6.3.2 Design Strategies of Fluorescent Redox Sensors and Key Examples -- 6.4 Conclusions -- References -- Chapter 7 Labelling Proteins and Biomolecules with Small Fluorescent Sensors -- 7.1 Labelling Biomolecules in Cells with Fluorescent Sensors -- 7.2 Small-molecule Modifications and Bioorthogonal Reactions -- 7.2.1 Polar Ketone and Aldehyde Condensations -- 7.2.2 Azide Bioorthogonal Chemistry -- 7.2.3 Tetrazine Ligation -- 7.2.4 Commercial Fluorescent Labels -- 7.3 Short peptide Recognition Sequences -- 7.4 Fusion Protein Tagging Systems -- 7.4.1 FKBP Tag -- 7.4.2 eDHFR Tag -- 7.4.3 PYP Tag. 7.4.4 SNAP-Tag and CLIP-Tag -- 7.4.5 HaloTag -- 7.5 Enzymatic Modifications for Labelling Proteins -- 7.5.1 The LAP-tag System -- 7.5.2 Protein Trans-splicing -- 7.6 Future Developments -- References -- Chapter 8 Future Directions of Fluorescence Sensors for Cellular Studies -- 8.1 Fluorescence Lifetime Imaging Microscopy -- 8.1.1 Introduction -- 8.1.2 Advantages of Fluorescence Lifetime Imaging Microscopy -- 8.1.3 Examples of Sensors for FLIM -- 8.1.4 Future Directions -- 8.2 Near-infrared Sensors -- 8.2.1 Strategies to Make NIR Sensors -- 8.2.2 NIR Fluorophore Scaffolds -- 8.2.3 Future Directions -- 8.3 Dual-analyte Sensing -- 8.3.1 Introduction -- 8.3.2 Recognition-Based Dual-analyte Sensors -- 8.3.3 Activity-based Dual-analyte Sensors -- 8.3.4 Mixed Dual-analyte Sensors -- 8.3.5 Sequence-specific Reactions -- 8.3.6 Conclusions and Future Directions -- 8.4 Super-resolution Microscopy -- 8.4.1 Introduction -- 8.4.2 Super-resolution Microscopy Techniques -- 8.4.3 Considerations for Use of Super Resolution Microscopy -- 8.4.4 Fluorescent Sensors for Super-resolution Microscopy -- 8.4.5 Future Directions -- 8.5 Multimodality -- 8.5.1 Introduction -- 8.5.2 Radioisotope Techniques -- 8.5.3 Computed Tomography -- 8.5.4 Magnetic Resonance Imaging -- 8.5.5 Photoacoustic Imaging -- 8.5.6 Vibrational Spectroscopy -- 8.5.7 Synchrotron X-ray Techniques -- 8.5.8 Mass Spectrometry -- 8.5.9 Electron Microscopy -- 8.5.10 Three or More Modalities -- 8.5.11 Future Directions -- References -- Index -- EULA. |
| Record Nr. | UNINA-9910677775003321 |
| Chichester, West Sussex, England ; ; Oxford, England : , : Wiley, , [2022] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular imaging [[electronic resource] ] : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day
| Molecular imaging [[electronic resource] ] : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day |
| Pubbl/distr/stampa | Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 |
| Descrizione fisica | 1 online resource (329 p.) |
| Disciplina | 570/.28 |
| Altri autori (Persone) |
PeriasamyAmmasi
DayRichard N |
| Collana | The American Physiological Society methods in physiology series |
| Soggetto topico |
Fluorescence microscopy
Fluorescence spectroscopy |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-281-03382-0
9786611033828 0-08-053687-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Molecular Imaging: FRET Microscopy and Spectroscopy; Copyright Page; Contents; Contributors; Chapter 1. Proteins and the Flow of Information in Cellular Function; Chapter 2. Basics of Fluorescence and FRET; Chapter 3. An Introduction to Filters and Mirrors for FRET; Chapter 4. FRET Imaging in the Wide-Field Microscope; Chapter 5. Confocal FRET Microscopy: Study of Clustered Distribution of Receptor-Ligand Complexes in Endocytic Membranes; Chapter 6. Multiphoton FRET Microscopy for Protein Localization in Tissue; Chapter 7. FRET Data Analysis: The Algorithm
Chapter 8. Photobleaching FRET MicroscopyChapter 9. Single-Molecule FRET; Chapter 10. FRET Measurements Using Multispectral Imaging; Chapter 11. Real-Time Fluorescence Lifetime Imaging and FRET Using Fast-Gated Image Intensifiers; Chapter 12. Streak Fluorescence Lifetime Imaging Microscopy: A Novel Technology for Quantitative FRET Imaging; Chapter 13. Time-Correlated Single Photon Counting Fluorescence Lifetime Imaging- FRET Microscopy for Protein Localization; Chapter 14. Bioluminescence Resonance Energy Transfer: Techniques and Potential Chapter 15. Quantifying Molecular Interactions with Fluorescence Correlation SpectroscopyChapter 16. Mapping Molecular Interactions and Transport in Cell Membranes by Image Correlation Spectroscopy; Index |
| Record Nr. | UNINA-9910458576903321 |
| Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular imaging [[electronic resource] ] : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day
| Molecular imaging [[electronic resource] ] : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day |
| Pubbl/distr/stampa | Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 |
| Descrizione fisica | 1 online resource (329 p.) |
| Disciplina | 570/.28 |
| Altri autori (Persone) |
PeriasamyAmmasi
DayRichard N |
| Collana | The American Physiological Society methods in physiology series |
| Soggetto topico |
Fluorescence microscopy
Fluorescence spectroscopy |
| ISBN |
1-281-03382-0
9786611033828 0-08-053687-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Molecular Imaging: FRET Microscopy and Spectroscopy; Copyright Page; Contents; Contributors; Chapter 1. Proteins and the Flow of Information in Cellular Function; Chapter 2. Basics of Fluorescence and FRET; Chapter 3. An Introduction to Filters and Mirrors for FRET; Chapter 4. FRET Imaging in the Wide-Field Microscope; Chapter 5. Confocal FRET Microscopy: Study of Clustered Distribution of Receptor-Ligand Complexes in Endocytic Membranes; Chapter 6. Multiphoton FRET Microscopy for Protein Localization in Tissue; Chapter 7. FRET Data Analysis: The Algorithm
Chapter 8. Photobleaching FRET MicroscopyChapter 9. Single-Molecule FRET; Chapter 10. FRET Measurements Using Multispectral Imaging; Chapter 11. Real-Time Fluorescence Lifetime Imaging and FRET Using Fast-Gated Image Intensifiers; Chapter 12. Streak Fluorescence Lifetime Imaging Microscopy: A Novel Technology for Quantitative FRET Imaging; Chapter 13. Time-Correlated Single Photon Counting Fluorescence Lifetime Imaging- FRET Microscopy for Protein Localization; Chapter 14. Bioluminescence Resonance Energy Transfer: Techniques and Potential Chapter 15. Quantifying Molecular Interactions with Fluorescence Correlation SpectroscopyChapter 16. Mapping Molecular Interactions and Transport in Cell Membranes by Image Correlation Spectroscopy; Index |
| Record Nr. | UNINA-9910784529103321 |
| Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular imaging : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day
| Molecular imaging : FRET microscopy and spectroscopy / / edited by Ammasi Periasamy, Richard N. Day |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 |
| Descrizione fisica | 1 online resource (329 p.) |
| Disciplina |
570/.28
570.28 |
| Altri autori (Persone) |
PeriasamyAmmasi
DayRichard N |
| Collana | The American Physiological Society methods in physiology series |
| Soggetto topico |
Fluorescence microscopy
Fluorescence spectroscopy |
| ISBN |
1-281-03382-0
9786611033828 0-08-053687-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Front Cover; Molecular Imaging: FRET Microscopy and Spectroscopy; Copyright Page; Contents; Contributors; Chapter 1. Proteins and the Flow of Information in Cellular Function; Chapter 2. Basics of Fluorescence and FRET; Chapter 3. An Introduction to Filters and Mirrors for FRET; Chapter 4. FRET Imaging in the Wide-Field Microscope; Chapter 5. Confocal FRET Microscopy: Study of Clustered Distribution of Receptor-Ligand Complexes in Endocytic Membranes; Chapter 6. Multiphoton FRET Microscopy for Protein Localization in Tissue; Chapter 7. FRET Data Analysis: The Algorithm
Chapter 8. Photobleaching FRET MicroscopyChapter 9. Single-Molecule FRET; Chapter 10. FRET Measurements Using Multispectral Imaging; Chapter 11. Real-Time Fluorescence Lifetime Imaging and FRET Using Fast-Gated Image Intensifiers; Chapter 12. Streak Fluorescence Lifetime Imaging Microscopy: A Novel Technology for Quantitative FRET Imaging; Chapter 13. Time-Correlated Single Photon Counting Fluorescence Lifetime Imaging- FRET Microscopy for Protein Localization; Chapter 14. Bioluminescence Resonance Energy Transfer: Techniques and Potential Chapter 15. Quantifying Molecular Interactions with Fluorescence Correlation SpectroscopyChapter 16. Mapping Molecular Interactions and Transport in Cell Membranes by Image Correlation Spectroscopy; Index |
| Record Nr. | UNINA-9910817984903321 |
| Oxford ; ; New York, : Published for the American Physiological Society by Oxford University Press, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular imaging and biology
| Molecular imaging and biology |
| Pubbl/distr/stampa | New York, NY, : Elsevier Science |
| Disciplina | 616 |
| Soggetto topico |
Diagnostic imaging
Fluorescence spectroscopy Molecular spectroscopy Diagnostic Imaging Molecular Biology Medicine Imagerie pour le diagnostic Spectroscopie de fluorescence Spectroscopie moléculaire |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1860-2002 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | MIB |
| Record Nr. | UNINA-9910134104703321 |
| New York, NY, : Elsevier Science | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Molecular imaging and biology
| Molecular imaging and biology |
| Pubbl/distr/stampa | New York, NY, : Elsevier Science |
| Disciplina | 616 |
| Soggetto topico |
Diagnostic imaging
Fluorescence spectroscopy Molecular spectroscopy Diagnostic Imaging Molecular Biology Medicine Imagerie pour le diagnostic Spectroscopie de fluorescence Spectroscopie moléculaire |
| Soggetto genere / forma | Periodicals. |
| ISSN | 1860-2002 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | MIB |
| Record Nr. | UNISA-996206147603316 |
| New York, NY, : Elsevier Science | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
The noninvasive analysis of painted surfaces : scientific impact and conservation practice / / edited by Austin Nevin and Tiarna Doherty
| The noninvasive analysis of painted surfaces : scientific impact and conservation practice / / edited by Austin Nevin and Tiarna Doherty |
| Pubbl/distr/stampa | Washington, D.C. : , : Smithsonian Institution Scholarly Press, , 2016 |
| Descrizione fisica | 1 online resource (viii, 81 pages) : color illustrations |
| Disciplina | 751.4 |
| Collana | Smithsonian contributions to museum conservation |
| Soggetto topico |
Painting - Conservation and restoration
Fluorescence spectroscopy Paint materials - Analysis Colorimetry |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Noninvasive analysis of painted surfaces |
| Record Nr. | UNINA-9910709693903321 |
| Washington, D.C. : , : Smithsonian Institution Scholarly Press, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
