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Titlebook: Advanced Fluorescence Microscopy; Methods and Protocol Peter J. Verveer Book 2015 Springer Science+Business Media New York 2015 biological

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发表于 2025-3-21 17:20:20 | 显示全部楼层 |阅读模式
期刊全称Advanced Fluorescence Microscopy
期刊简称Methods and Protocol
影响因子2023Peter J. Verveer
视频video
发行地址Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts.Includes supplementary materia
学科分类Methods in Molecular Biology
图书封面Titlebook: Advanced Fluorescence Microscopy; Methods and Protocol Peter J. Verveer Book 2015 Springer Science+Business Media New York 2015 biological
影响因子.This volume provides an overview of advanced  fluorescence microscopy, covering a broad range of methods. Each chapter focuses on a different method and provides a practical guide for application in biological systems.  Written in the highly successful .Methods in Molecular Biology . series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls..Authoritative and cutting-edge,  .Advanced Fluorescence Microscopy: Methods and Protocols. seeks to provide scientists with methods for biological systems that are of interest. .
Pindex Book 2015
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发表于 2025-3-21 23:55:50 | 显示全部楼层
Die ertragsteuerliche Organschaftquestions. We explain technical aspects of sample preparation and image acquisition that will help in obtaining good diffraction-unlimited pictures. We also present embedding techniques adapted for ultrathin sectioning, which allow optimal 3D resolutions in virtually all biological preparations.
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https://doi.org/10.1007/978-3-642-51985-7commercial system. We explain how TIRF can be combined with other microscopy modalities and describe how to use TIRF to study processes such as endocytosis, exocytosis, and focal adhesion dynamics. Finally, we provide a step-by-step guide to imaging and analyzing focal adhesion dynamics in a migrating cell using TIRF microscopy.
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https://doi.org/10.1007/978-3-322-85310-3signaling events inside living cells, e.g., Protein–Protein interactions. In this chapter, we describe the calibration of both time-correlated single-photon counting (TCSPC) and frequency domain (FD) FLIM systems and the acquisition and analysis of FLIM-FRET data for investigating Protein–Protein interactions in living cells.
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https://doi.org/10.1007/978-3-322-85310-3ipt language. The simulation tool fits very well in a systems biology research setting that aims to maintain an interactive cycle of experiment-driven modelling and model-driven experimentation: the model and the experiment are in the same simulation. The full program can be obtained by request to the authors.
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