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Titlebook: Cytoskeleton Methods and Protocols; Ray H. Gavin Book 2016Latest edition Springer Science+Business Media New York 2016 Cell and Organelle

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發(fā)表于 2025-3-21 17:19:23 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Cytoskeleton Methods and Protocols
編輯Ray H. Gavin
視頻videohttp://file.papertrans.cn/243/242681/242681.mp4
概述Includes cutting-edge methods and protocols.Provides step-by-step detail essential for reproducible results.Contains key notes and implementation advice from the experts
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Cytoskeleton Methods and Protocols;  Ray H. Gavin Book 2016Latest edition Springer Science+Business Media New York 2016 Cell and Organelle
描述.The third edition of this volume focuses on experimental models that are useful for investigating various aspects of cytoskeleton structure and function. Animal, plant, protist, and fungal models highlight twenty-four chapters that provide detailed protocols for live and fixed-cell imaging, dynamics of cytoskeleton components, cell and organelle motility, and genetics and proteomics. Written in the highly successful .Methods in Molecular Biology .series format, protocols in each chapter are up-to-date menus organized in a useful step-by-step format appropriate for novice and established investigators. Each chapter is equipped with a valuable notes section that provides a troubleshooting guide and helpful, and often unpublished, technical information aimed at ensuring success with implementation of the protocols..Authoritative and thorough, .Cytoskeleton Methods and Protocols, Third Edition. helps researchers expand their understanding of cytoskeleton structure and function..
出版日期Book 2016Latest edition
關(guān)鍵詞Cell and Organelle Motility; Cell-Imaging; Cytoskeleton Components; Cytoskeleton Function; Cytoskeleton
版次3
doihttps://doi.org/10.1007/978-1-4939-3124-8
isbn_softcover978-1-4939-4975-5
isbn_ebook978-1-4939-3124-8Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightSpringer Science+Business Media New York 2016
The information of publication is updating

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發(fā)表于 2025-3-21 22:54:33 | 只看該作者
Live-Cell Imaging of Mitochondria and the Actin Cytoskeleton in Budding Yeastgeneration and muscle myopathies, and overall cellular aging are marked by declining mitochondrial function and subsequent loss of multiple other cellular functions. For these reasons, optimized protocols are needed for visualization and quantification of mitochondria and their function and fitness.
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發(fā)表于 2025-3-22 03:55:16 | 只看該作者
Imaging of the Actin Cytoskeleton and Mitochondria in Fixed Budding Yeast Cellsshape, and rigid cell wall created obstacles to explore the cell biology of this model eukaryote. It is now possible to acquire and analyze high-resolution and super-resolution multidimensional images of the yeast cell. As a result, imaging of yeast has emerged as an important tool in eukaryotic cel
地板
發(fā)表于 2025-3-22 07:11:39 | 只看該作者
Imaging of the Cytoskeleton Using Live and Fixed , Tissue Culture Cellsm. Their ease of culture and maintenance, susceptibility to RNA interference, and imaging characteristics have led to extensive use in both traditional experimental approaches as well as high-throughput RNAi screens. Here we describe . S2 cell culture and preparation for live-cell and fixed-cell flu
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發(fā)表于 2025-3-22 11:44:13 | 只看該作者
Imaging Cytoskeleton Components by Electron Microscopyical properties of a cell. Fibrillar polymers—actin filaments, microtubules, and intermediate filaments—are major constituents of the cytoskeleton, which constantly change their organization during cellular activities. The actin cytoskeleton is especially polymorphic, as actin filaments can form mul
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發(fā)表于 2025-3-22 14:17:08 | 只看該作者
Purification and Localization of Intraflagellar Transport Particles and PolypeptidesThis includes the primary cilia of most human cells that are in the G. phase of the cell cycle. The model system for the study of IFT is the flagella of the biflagellate green alga .. It is in this organism that IFT was first discovered, and genetic data from a . mutant first linked the process of I
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發(fā)表于 2025-3-22 20:59:25 | 只看該作者
Fluorescence Imaging of the Cytoskeleton in Plant Rootsowever, to make full use of these live cell reporters it is necessary to implement simple methods to maintain plant specimens in optimal growing conditions during imaging. To image the cytoskeleton in living Arabidopsis roots, we rely on a system involving coverslips coated with nutrient supplemente
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發(fā)表于 2025-3-22 22:12:06 | 只看該作者
Microtubules in Plant Cells: Strategies and Methods for Immunofluorescence, Transmission Electron Minalyze them. This chapter provides specific methods that can be used to analyze microtubule organization and dynamic properties in plant systems and summarizes the advantages and limitations for each technique. We outline basic methods for preparing samples for immunofluorescence labeling, including
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發(fā)表于 2025-3-23 04:54:02 | 只看該作者
Basic Methods to Visualize Actin Filaments In Vitro Using Fluorescence Microscopy for Observation ofry to characterize effects of the protein on actin filament dynamics in vitro. This chapter describes basic microscopic methods to visualize fluorescently labeled actin filaments using commonly available fluorescence microscope settings. Direct microscopic observation of actin filaments provides str
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發(fā)表于 2025-3-23 07:28:32 | 只看該作者
An In Vitro Model System to Test Mechano-microbiological Interactions Between Bacteria and Host Celle developed an in vitro system that combines micromanipulation of force by magnetic tweezers with simultaneous live cell fluorescence microscopy. We applied pulling forces to magnetic beads coated with the . Type IV pili in the same order of magnitude than the forces generated by live bacteria. We s
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