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

麻煩

書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols影響因子(影響力)




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols被引頻次




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols被引頻次學(xué)科排名




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols年度引用




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols年度引用學(xué)科排名




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols讀者反饋




書(shū)目名稱(chēng)Cytoskeleton Methods and Protocols讀者反饋學(xué)科排名

humectant

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.

spondylosis

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

strain

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

匯總

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

GENUS

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

GENUS

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

Favorable

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

放大

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

Disk199

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