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  • 1
    UID:
    almahu_9948595847402882
    Format: 1 online resource (697 p.)
    Edition: 2nd ed.
    ISBN: 1-281-05700-2 , 9786611057008 , 0-08-053177-6
    Series Statement: Biological techniques
    Content: The use of fluorescent and luminescent probes to measure biological function has increased dramatically since publication of the First Edition due to their improved speed, safety, and power of analytical approach. This eagerly awaited Second Edition, also edited by Bill Mason, contains 19 new chapters and over two thirds new material, and is a must for all life scientists using optical probes.The contents include discussion of new optical methodologies for detection of proteins, DNA and other molecules, as well as probes for ions, receptors, cellular components, and gene expression. Emergi
    Note: Description based upon print version of record. , Front Cover; Fluorescent and Luminescent Probes for Biological Activity: A Practical Guide to Technology for Quantitative Real-Time Analysis; Copyright Page; Series Preface; Preface; Contributors; Contents; Part I: Introduction to Fluorescence Microscopy; Chapter One. Fluorescence Microscopy; 1.1 Introduction; 1.2 Microscope design; 1.3 Types of illumination; 1.4 Light sources; 1.5 Filters; 1.6 Objectives and eyepieces; References; Part II: Optical Probes and Their Applications; Chapter Two. Introduction to Fluorescent Probes: Properties, History and Applications; 2.1 Introduction , 2.2 Nature of fluorescence and properties of fluorescent probes2.3 Historical developments; 2.4 Applications of fluorochromes in histology and microbiology; 2.5 Introduction of acridine orange into cell physiology, cytology and cytochemistry; 2.6 General applications of fluorescent probes; Acknowledgements; References; Chapter Three. Intracellular Ion Indicators; 3.1 Introduction; 3.2 General properties of intracellular ion indicators; 3.3 Examples of intracellular ion indicators; 3.4 Conclusions; Acknowledgements; References , Chapter Four. Fluorescent Imaging of Nucleic Acids and Proteins in Gels4.1 Introduction; 4.2 General properties of fluorescent nucleic acid stains; 4.3 Examples of fluorescent nucleic acid gel stains; 4.4 General properties of fluorophore labels used to detect nucleic acids; 4.5 General properties of fluorescent protein gel stains; 4.6 Examples of fluorescent protein gel stains; 4.7 Protein labelling; 4.8 Conclusions; Acknowledgements; References; Part III: Using Optical Probes in Cells - Practicalities, Problems and Pitfalls , Chapter Five. Introducing and Calibrating Fluorescent Probes in Cells and Organelles5.1 Introduction; 5.2 General principles of the loading process; 5.3 General principles of the calibration process; 5.4 Putting principles into practice; Acknowledgements; References; Chapter Six. Electroporation: A Method for Introduction of Non-permeable Molecular Probes; 6.1 Introduction; 6.2 Basic concept of electroporation; 6.3 Electric field generation and monitoring; 6.4 Polarization of the outer membrane; 6.5 Electropore formation and resealing; 6.6 Transmembrane transport , 6.7 Practical considerations of electroporation6.8 Experimental evidence; 6.9 Summary; Acknowledgements; References; Chapter Seven. Imaging Reality: Understanding Maps of Physiological Cell Signals Measured by Fluorescence Microscopy and Digital Imaging; 7.1 Introduction; 7.2 Generic considerations for the use of fluorescent indicators; 7.3 Optimization of fluorescent light detection and background light correction; 7.4 3-D spatial maps of fluorescent signals; Acknowledgements; References; Chapter Eight. Fluorescent Probes in Practice - Potential Artifacts; 8.1 Introduction , 8.2 Photobleaching , English
    Additional Edition: ISBN 0-12-447836-0
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    b3kat_BV012639781
    Format: XXV, 647 S. , Ill., graph. Darst.
    Edition: 2. ed.
    ISBN: 0124478360
    Series Statement: Biological techniques
    Language: English
    Subjects: Biology
    RVK:
    RVK:
    Keywords: Fluoreszenzmarkierung ; Fluoreszenzmikroskopie ; Durchflusscytometrie
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    UID:
    almahu_BV025309662
    Format: XXV, 647 S. : , Ill., graph. Darst.
    Edition: 2nd ed.
    ISBN: 0-12-447836-0
    Series Statement: Biological techniques
    Language: English
    Subjects: Chemistry/Pharmacy , Biology
    RVK:
    RVK:
    RVK:
    Keywords: Fluoreszenzmarkierung ; Fluoreszenzmikroskopie ; Durchflusscytometrie
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    UID:
    edoccha_BV042305348
    Format: 1 Online-Ressource (XXV, 647 S.) : , Ill., graph. Darst.
    Edition: 2. ed.
    ISBN: 0-12-447836-0 , 978-0-12-447836-7 , 978-0-08-053177-9
    Series Statement: Biological techniques
    Note: The use of fluorescent and luminescent probes to measure biological function has increased dramatically since publication of the First Edition due to their improved speed, safety, and power of analytical approach. This eagerly awaited Second Edition, also edited by Bill Mason, contains 19 new chapters and over two thirds new material, and is a must for all life scientists using optical probes. The contents include discussion of new optical methodologies for detection of proteins, DNA and other molecules, as well as probes for ions, receptors, cellular components, and gene expression. Emerging and advanced technologies for probe detection such as confocal laser scanning microscopy are also covered. This book will be essential for those embarking on work in the field or using new methods to enhance their research. TOPICS COVERED: * Single and multiphoton confocal microscopy * Applications of green fluorescent protein and chemiluminescent reporters to gene expression studies * Applications of new optical probes for imaging proteins in gels * Probes and detection technologies for imaging membrane potential in live cells * Use of optical probes to detect microorganisms * Raman and confocal raman microspectroscopy * Fluorescence lifetime imaging microscopy * Digital CCD cameras and their application in biological microscopy
    Language: English
    Keywords: Fluoreszenzmarkierung ; Fluoreszenzmikroskopie ; Durchflusscytometrie
    Library Location Call Number Volume/Issue/Year Availability
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  • 5
    UID:
    edocfu_BV042305348
    Format: 1 Online-Ressource (XXV, 647 S.) : , Ill., graph. Darst.
    Edition: 2. ed.
    ISBN: 0-12-447836-0 , 978-0-12-447836-7 , 978-0-08-053177-9
    Series Statement: Biological techniques
    Note: The use of fluorescent and luminescent probes to measure biological function has increased dramatically since publication of the First Edition due to their improved speed, safety, and power of analytical approach. This eagerly awaited Second Edition, also edited by Bill Mason, contains 19 new chapters and over two thirds new material, and is a must for all life scientists using optical probes. The contents include discussion of new optical methodologies for detection of proteins, DNA and other molecules, as well as probes for ions, receptors, cellular components, and gene expression. Emerging and advanced technologies for probe detection such as confocal laser scanning microscopy are also covered. This book will be essential for those embarking on work in the field or using new methods to enhance their research. TOPICS COVERED: * Single and multiphoton confocal microscopy * Applications of green fluorescent protein and chemiluminescent reporters to gene expression studies * Applications of new optical probes for imaging proteins in gels * Probes and detection technologies for imaging membrane potential in live cells * Use of optical probes to detect microorganisms * Raman and confocal raman microspectroscopy * Fluorescence lifetime imaging microscopy * Digital CCD cameras and their application in biological microscopy
    Language: English
    Keywords: Fluoreszenzmarkierung ; Fluoreszenzmikroskopie ; Durchflusscytometrie
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
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