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Microwave fixation improves antigenicity of glutaraldehyde-sensitive antigens while preserving ultrastructural detail.
Author(s) -
Maria Célia Jamur,
Cloris D. Faraco,
Laurelúcia Orive Lunardi,
R P Siraganian,
Constance Oliver
Publication year - 1995
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/43.3.7868860
Subject(s) - glutaraldehyde , antigenicity , immunocytochemistry , ultrastructure , antigen retrieval , fixation (population genetics) , antigen , bone marrow , immunostaining , microbiology and biotechnology , biology , chemistry , monoclonal antibody , pathology , immunology , immunohistochemistry , antibody , biochemistry , anatomy , medicine , gene
Microwave fixation for electron microscopy has been used primarily for post-embedding immunocytochemistry. The present study examined the ability of microwave fixation to preserve the antigenicity of glutaraldehyde-sensitive antigens for pre-embedding immunocytochemistry. Five monoclonal antibodies (MAbs) directed against cell surface components of rat mast cells were tested. The MAbs failed to show any labeling of conventionally fixed rat bone marrow-derived mast cells even at glutaraldehyde concentrations as low as 0.1%. Strong staining of mast cell plasma membranes was seen when bone marrow was initially fixed with 2% formaldehyde and then refixed in 2% glutaraldehyde/2% formaldehyde after immunostaining. However, the ultrastructural preservation of the cells was poor. Antigenicity and morphological detail were both preserved when bone marrow was fixed in 0.05% glutaraldehyde/2% formaldehyde for 4 sec in a 550-W microwave oven. With this method, mast cells in various stages of maturation as well as cells that did not contain granules were immunoreactive. This method should prove useful with antigens from many different cell types that are sensitive to glutaraldehyde fixation.

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