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141222 ||| eng |
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|a 9780123858733
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|a 0123858739
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|a 9781282257429
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|a 1282257420
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|a 9780123858726
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|a 0123858720
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| 100 |
1 |
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|a Wouterlood, Floris G.
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| 245 |
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|a Cellular imaging techniques for neuroscience and beyond
|h [electronic resource]
|h Elektronische Ressource
|c Floris G. Wouterlood, editor
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| 260 |
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|a Amsterdam
|b Elsevier/Academic Press
|c 2012, 2012
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| 300 |
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|a online resource (xiii, 282 pages, [21] pages of plates)
|b illustrations
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| 505 |
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|a Includes bibliographical references and index
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|a of Instrument, Computer Processing, and Men; Introduction; Pinhole, Depth of Focus, and Laser Illumination; When/Why Does One Need a CLSM?; Abbe, Shannon, and Nyquist; Imaging of a 2D Line and Deblurring; Axial Resolution; Resolution and Sampling; Signal Separation, Orders of Magnitude, and Resolution Limits; Confocal Microscopy Further Considered; Cross Talk Awareness; Excitation Cross Talk; Elimination of Cross Talk
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| 505 |
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|a Extra Marker; Colocalization; Conclusion; Acknowledgments; References; 2 Beyond Abbe's Resolution Barrier: STED Microscopy; Introduction; A New Wave of Imaging; STED Microscopy: The Basic Concept; Implementation of STED Microscopy; The Microscope Base; Laser Sources; The Doughnut; Synchronization
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| 505 |
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|a Speed, Color, Depth, Live Imaging; Temporal Resolution and Imaging Speed; Labeling Strategies; Multicolor Imaging; Depth Penetration and Spatial Resolution; Spatial Resolution in z; Live-cell Imaging; Summary and Outlook; Reversible Saturable Optical Fluorescence Transitions: A More General Principle for Nanoscopy; Other Areas of Development; References; 3 Enhancement of Optical Resolution by 4pi Single and Multiphoton Confocal Fluorescence Microscopy; Introduction
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| 505 |
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|a The 4pi Principle and SetupMicroscope Alignment; Initial Alignment of the Excitation by Eye; Optimizing the Coverslip Correction Ring; Alignment of the Bottom Lens (XYZ); Alignment of the Second Mirror (XYZ); 4pi Imaging; 4pi Deconvolution; Sample Preparation; Fixation; Selection of Fluorescent Dyes; Microtubule and Microtubule Plus End Imaging; Visualization of DNA; 4pi Imaging of Muntjac Chromosomes; Single-photon Excitation (Measurement of the Redox State in Dopamine Neurons); SYCP3 Axis as a Marker for Chromatin Organization in Mouse Spermatocytes; Microbubbles with Medicine
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| 505 |
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|a PALM and FPALM; Using a Pair of Interacting Cyanine Dyes: STORM; Using Blinking Dyes: dSTORM; Using High-intensity Light: GSDIM; Using Targeted Molecules: BALM.
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| 653 |
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|a Diagnostic imaging / Methods
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| 653 |
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|a Cytology / Methodology
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| 653 |
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|a Microscopy
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| 653 |
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|a Neurosciences
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| 653 |
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|a Diagnostic Imaging / methods
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| 653 |
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|a Neurosciences
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| 653 |
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|a Medicine
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| 653 |
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|a MEDICAL / Diagnosis / bisacsh
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| 653 |
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|a MEDICAL / Diagnostic Imaging / bisacsh
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| 653 |
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|a Cytology / Methodology / fast / (OCoLC)fst00886294
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| 653 |
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|a Diagnostic imaging / fast / (OCoLC)fst00892354
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| 653 |
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|a Microscopy / fast / (OCoLC)fst01020062
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| 653 |
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|a Neurosciences / fast / (OCoLC)fst01036509
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| 041 |
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7 |
|a eng
|2 ISO 639-2
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| 989 |
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|b ESD
|a Elsevier ScienceDirect eBooks
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| 856 |
4 |
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|u http://www.sciencedirect.com/science/book/9780123858726
|x Verlag
|3 Volltext
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| 082 |
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|a 616.0754
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| 520 |
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|a The imaging of small cellular components requires powerful instruments, and an entire family of equipment and techniques based on the confocal principle has been developed over the past 30 years. Such methods are commonly used by neuroscience researchers, but the majority of these users do not have a microscopy or a cell biology backgrounds and do can encounter difficulties in obtaining and interpreting results. This volume brings experts in high-resolution optical microscopy applications in neuroscience and cell biology together to document the state of the art. Outlining what is currently possible, the volume also discusses promising developments for the future and aids readers in selecting the most scientifically meaningful approach to solve their questions. Each chapter discusses instrumentation and technology in relationship to application in research. All of the common and cutting edge trends are covered - fluorescence / laser electron / nonlinear microscopy, infrared fluorescence, multiphoton imaging, tomography, FRAP, live imaging, STED, PALM/STORM, etc. * The first comprehensive volume on cellular imaging with a focus for its application in neuroscience * Concluding chapter compares the merits of various techniques * Full color throughout, maximizing users comprehension of the results obtainable via various methods * Features outstanding and truly international scholarship, with chapters written by leading experts in neuroscience and cell biology * Discusses cutting edge methods such as STED, PALM/STORM, nonlinear microscopy and more
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