Optimal Processing Method to Obtain Four-color Confocal Fluorescent Images of the Cytoskeleton and Nucleus in Three-dimensional Chondrocyte Cultures
Author:
Affiliation:
1. Department of Chemical Engineering (AB,MDB), Ecole Polytechnique, Montreal, Quebec, Canada
2. Institute of Biomedical Engineering (NT-K,DF,MDB), Ecole Polytechnique, Montreal, Quebec, Canada
Abstract
Publisher
SAGE Publications
Subject
Histology,Anatomy
Link
http://journals.sagepub.com/doi/pdf/10.1369/jhc.5B6728.2005
Reference9 articles.
1. Visualization of Prosomes (MCP-Proteasomes), Intermediate Filament and Actin Networks by “Instantaneous Fixation” Preserving the Cytoskeleton
2. Guiding Principles of Specimen Preservation for Confocal Fluorescence Microscopy
3. Multi-Spectral Imaging and Linear Unmixing Add a Whole New Dimension to Laser Scanning Fluorescence Microscopy
4. Mature Full-thickness Articular Cartilage Explants Attached to Bone are Physiologically Stable over Long-term Culture in Serum-free Media
5. Organisation of the chondrocyte cytoskeleton and its response to changing mechanical conditions in organ culture
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