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Titlebook: Basic Confocal Microscopy; W. Gray (Jay) Jerome,Robert L. Price Book 2018Latest edition Springer Nature Switzerland AG 2018 fluorescence.m

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發(fā)表于 2025-3-21 16:22:27 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Basic Confocal Microscopy
影響因子2023W. Gray (Jay) Jerome,Robert L. Price
視頻videohttp://file.papertrans.cn/181/180996/180996.mp4
發(fā)行地址Fully updated and expanded to reflect developments in the field yet still concise and comprehensive.Covers the basics needed to design, implement, and interpret the results of biological experiments b
圖書封面Titlebook: Basic Confocal Microscopy;  W. Gray (Jay) Jerome,Robert L. Price Book 2018Latest edition Springer Nature Switzerland AG 2018 fluorescence.m
影響因子.Basic Confocal Microscopy.,?Second Edition?builds on the successful first edition by keeping the same format and reflecting relevant changes and recent developments in this still-burgeoning field. This format is based on the Confocal Microscopy Workshop that has been taught by several of the authors for nearly 20 years and remains a popular workshop for gaining basic skills in confocal microscopy. While much of the information concerning fluorescence and confocal microscopy that made the first edition a success has not changed in the six years since the book was first published, confocal imaging is an evolving field and recent advances in detector technology, operating software, tissue preparation and clearing, image analysis, and more have been updated to reflect this. Several of these advances are now considered routine in many laboratories, and others such as super resolution techniques built on confocal technology are becoming widely available.??.
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Faalangst/examenvrees van (t)huis uit,croscope. The most important modifications are (1) a strong illumination system that provides suitable wavelengths for exciting a specific fluorochrome, (2) some mechanism to limit the illumination beam to specific wavelengths so that only the fluorochrome of choice is excited, and (3) a means to im
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Onderhandelen in partnerrelatietherapie,ent when visualized in brightfield or various types of interference-based light microscopy (LM). However, for the unambiguous identification and localization of most biological molecular or macromolecular elements within a structural framework, some type of staining/labeling must be employed. This i
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