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Keratin filaments are a hallmark of epithelial differentiation. Their cell type-specific spatial organization and dynamic properties reflect and support epithelial function. To study this interdependency, imaging of fluorescently tagged keratins is a widely used method by which the temporospatial organization and behavior of the keratin intermediate filament network can be analyzed in living cells. Here, we describe methods that have been adapted and optimized to dissect and quantify keratin intermediate filament network dynamics in vital cultured cells and functional tissues. Copyright © 2016 Elsevier Inc. All rights reserved.

Citation

Nicole Schwarz, Marcin Moch, Reinhard Windoffer, Rudolf E Leube. Multidimensional Monitoring of Keratin Intermediate Filaments in Cultured Cells and Tissues. Methods in enzymology. 2016;568:59-83


PMID: 26795467

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