Cellular Imaging Techniques for Neuroscience and Beyond
Nonfiction, Science & Nature, Science, Biological Sciences, Cytology
| Author: | ISBN: | 9780123858733 | |
| Publisher: | Elsevier Science | Publication: | December 6, 2012 |
| Imprint: | Academic Press | Language: | English |
| Author: | |
| ISBN: | 9780123858733 |
| Publisher: | Elsevier Science |
| Publication: | December 6, 2012 |
| Imprint: | Academic Press |
| Language: | English |
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.
- Single and multiphoton confocal microscopy, and 4-pi confocal microscopy
- Obtaining nanoresolution via photoactivation localization microscopy (PALM)
- Several procedures that correlate observations in optical fluorescence microscopy and electron microscopy
- Study of morphology and function via high-resolution fluorescence procedures
- Additional high-resolution microscopic techniques
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.
- Single and multiphoton confocal microscopy, and 4-pi confocal microscopy
- Obtaining nanoresolution via photoactivation localization microscopy (PALM)
- Several procedures that correlate observations in optical fluorescence microscopy and electron microscopy
- Study of morphology and function via high-resolution fluorescence procedures
- Additional high-resolution microscopic techniques
