| Literature DB >> 29310772 |
Douglas R Keene1, Sara F Tufa2.
Abstract
This chapter gives insight into task-specific methodologies for the evaluation of matrix ultrastructure by light and electron microscopy. It separately considers the isolation and preparation of molecular isolates for negative staining, immunolabeling, rotary shadowing, and single particle analysis. Also considered is the preparation of whole tissues and cultured cells by chemical fixation and cryofixation methodologies. Immunoelectron microscopy for immunoidentification of matrix components may be accomplished en bloc or via section-surface protocols; the advantages and pitfalls in both methodologies are described. Correlative light and electron microscopy, particularly utilizing GFP constructs, demands special consideration in fixation and embedding protocols. TEM imaging methods, including the use of montage software and the acquisition of thick-section tilt series are discussed. The protocols presented in this chapter, with the exception of single particle analysis, are those which are continuously used in our laboratory and represent the latest modifications in our protocols.Keywords: Aorta; Cartilage; Connective tissue matrix; Correlative light and electron microscopy; Cryo; Fixation protocol; High-pressure freezing; Immunolabeling; Skin; Tendon; Transmission electron microscopy
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Year: 2017 PMID: 29310772 DOI: 10.1016/bs.mcb.2017.08.002
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441