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THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody

Antibody staining was observed in the electron microscope by means of untagged antibody and osmium fixation. The antibody was visualized as a change in morphology due to its deposition on the antigenic structures. Glycerinated chicken breast muscle was stained with antimyosin, anti-H-meromyosin, and...

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Detalles Bibliográficos
Autores principales: Pepe, Frank A., Finck, H., Holtzer, H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1961
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2225137/
https://www.ncbi.nlm.nih.gov/pubmed/14485151
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author Pepe, Frank A.
Finck, H.
Holtzer, H.
author_facet Pepe, Frank A.
Finck, H.
Holtzer, H.
author_sort Pepe, Frank A.
collection PubMed
description Antibody staining was observed in the electron microscope by means of untagged antibody and osmium fixation. The antibody was visualized as a change in morphology due to its deposition on the antigenic structures. Glycerinated chicken breast muscle was stained with antimyosin, anti-H-meromyosin, and antiactin. The staining patterns obtained by electron microscopy were consistent with those previously demonstrated by fluorescence microscopy. A second method was used for confirmation of antibody staining. This consisted of extraction of unstained portions of the sarcomere with 0.6 M potassium iodide, 10(-4) M adenosine triphosphate solution. Stained regions of the sarcomere remained intact because of insolubility of the combined antigen and antibody.
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spelling pubmed-22251372008-05-01 THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody Pepe, Frank A. Finck, H. Holtzer, H. J Biophys Biochem Cytol Article Antibody staining was observed in the electron microscope by means of untagged antibody and osmium fixation. The antibody was visualized as a change in morphology due to its deposition on the antigenic structures. Glycerinated chicken breast muscle was stained with antimyosin, anti-H-meromyosin, and antiactin. The staining patterns obtained by electron microscopy were consistent with those previously demonstrated by fluorescence microscopy. A second method was used for confirmation of antibody staining. This consisted of extraction of unstained portions of the sarcomere with 0.6 M potassium iodide, 10(-4) M adenosine triphosphate solution. Stained regions of the sarcomere remained intact because of insolubility of the combined antigen and antibody. The Rockefeller University Press 1961-12-01 /pmc/articles/PMC2225137/ /pubmed/14485151 Text en Copyright © Copyright, 1961, by The Rockefeller Institute Press
spellingShingle Article
Pepe, Frank A.
Finck, H.
Holtzer, H.
THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title_full THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title_fullStr THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title_full_unstemmed THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title_short THE USE OF SPECIFIC ANTIBODY IN ELECTRON MICROSCOPY : III. Localization of Antigens by the Use of Unmodified Antibody
title_sort use of specific antibody in electron microscopy : iii. localization of antigens by the use of unmodified antibody
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2225137/
https://www.ncbi.nlm.nih.gov/pubmed/14485151
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