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Titlebook: Handbook of Biological Confocal Microscopy; James B. Pawley Book 1990 Springer Science+Business Media New York 1990 biology.cell.developme

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书目名称Handbook of Biological Confocal Microscopy
编辑James B. Pawley
视频video
图书封面Titlebook: Handbook of Biological Confocal Microscopy;  James B. Pawley Book 1990 Springer Science+Business Media New York 1990 biology.cell.developme
描述In 1987 the Electron Microscopy Society of America (EMSA) going to drive important scientific discoveries across wide areas under the leadership of J. P. Revel (Cal Tech) initiated a major of physiology, cellular biology and neurobiology. They had been program to present a discussion of recent advances in light looking for a forum in which they could advance the state of microscopy as part of the annual meeting. The result was three the art of confocal microscopy, alert manufacturers to the lim­ special LM sessions at the Milwaukee meeting in August 1988: itations of current instruments, and catalyze progress toward The LM Forum, organized by me, and Symposia on Confocal new directions in confocal instrument development. LM, organized by G. Schatten (Madison), and on Integrated These goals were so close to those of the EMSA project that Acoustic/LM/EM organized by C. Rieder (Albany). In addition, the two groups decided to join forces with EMSA to provide there was an optical micro-analysis session emphasizing Raman the organization and the venue for a Confocal Workshop and techniques, organized by the Microbeam Analysis Society, for NSF to provide the financial support for the spea
出版日期Book 1990
关键词biology; cell; development; electron microscopy; microscopy; neurobiology; organizations; physiology
版次1
doihttps://doi.org/10.1007/978-1-4615-7133-9
isbn_ebook978-1-4615-7133-9
copyrightSpringer Science+Business Media New York 1990
The information of publication is updating

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https://doi.org/10.1007/978-1-4615-7133-9biology; cell; development; electron microscopy; microscopy; neurobiology; organizations; physiology
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Pneumothorax. Chronische Phthise,inition and the contrast of the image are better than with a standard microscope, the device is very well-suited for optical cross-sectioning, and with the use of a laser beam, the intensity of illumination can be very high. At the same time, it is possible to choose the wavelength of the illumination very easily [Wilson et al, 1984].
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https://doi.org/10.1007/978-1-935704-14-0 illumination and imaging systems. Other aperture shapes can of course be utilized, and the slit is an attractive alternative. In a number of circumstances the slit aperture confocal system can have advantages over circular aperture systems.
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