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Titlebook: Methods in Plant Electron Microscopy and Cytochemistry; William V. Dashek Book 2000 Springer Science+Business Media New York 2000 Organe.P

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发表于 2025-3-21 18:32:10 | 显示全部楼层 |阅读模式
书目名称Methods in Plant Electron Microscopy and Cytochemistry
编辑William V. Dashek
视频video
概述Includes supplementary material:
图书封面Titlebook: Methods in Plant Electron Microscopy and Cytochemistry;  William V. Dashek Book 2000 Springer Science+Business Media New York 2000 Organe.P
描述Hands-on experimentalists describe the cutting-edge microscopical methods needed for the effective study of plant cell biology today. These powerful techniques, all described in great detail to ensure successful experimental results, range from light microscope cytochemistry, autoradiography, and immunocytochemistry, to recent developments in fluorescence, confocal, and dark-field microscopies. Important advances in both conventional and scanning electron microscopies are also fully developed, together with such state-of-the-art ancillary techniques as high-resolution autoradiography, immunoelectron microscopy, X-ray microanalysis, and electron systems imaging. Easy-to-use and up-to-date, Methods in Plant Electron Microscopy and Cytochemistry offers today‘s plant scientists a first class collection of readily reproducible light and electron microscopical methods that will prove the new standard for all working in the field.
出版日期Book 2000
关键词Organe; Polle; biology; development; plant
版次1
doihttps://doi.org/10.1007/978-1-59259-232-6
isbn_softcover978-0-89603-809-7
isbn_ebook978-1-59259-232-6
copyrightSpringer Science+Business Media New York 2000
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Methods in Light Microscope Radioautography,topes dose and route of administration) to cells, tissues in culture, or even whole tissues followed by the preparation of sections from paraffin/paraplast or resin-embedded specimens . Chapter 2). The sections are coated with the appropriate fine grain, photographic emulsion . Table 1) and the sect
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Dark-Field Microscopy and Its Application to Pollen Tube Culture,tly enters the light path of the objective lens . Fig. 1A). Only the scattered light by the specimen enters the objective lens . Fig. 1C). Specimen features thus appear bright on a dark background. When a powerful light source such as a mercury lamp is used for illumination, small objects can be det
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Computer-Assisted Microphotometry,r and a few accessories to a light microscope, and it may be possible to quantify a cytochemical reaction product, measure the spectrum of a pigment, quantify natural or induced fluorescence, quantify birefringence, or map and analyze an image. But manually collecting thousands of numbers is unbelie
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