A simple method for coupling in situ hybridization and immunocytochemistry: application to the study of peptidergic neuronsC Bugnon, M Bahjaoui and D Fellmann Laboratoire d'Histologie-Embryologie-Cytogenetique, CNRS URA 561, Universite de Franche-Comte, Faculte de Medecine, Besancon, France. We have devised a simple procedure for immunostaining of sections that have previously undergone autoradiographic visualization of mRNAs by in situ hybridization. Classical hybridocytochemistry techniques were performed first on cryostat sections of formaldehyde-fixed tissue. Standard methods were used for slide coating by emulsion dipping and for revelation, fixation, and coverslipping steps. The key to this method is the emulsion removal, or permeabilization, by a short trypsin incubation (0.2% for 20-30 sec) which facilitates the good access of antibodies used in a subsequent immunocytochemical technique to section epitopes. Usual immunofluorescence and immunoperoxidase procedures were successfully performed after this treatment. The immunoreactivity of several neuropeptides was well preserved after this procedure. In addition to its usefulness in our studies, this general method should be applicable to many other situations in which autoradiographic and immunocytochemical detections must be coupled.
Volume 39,
Issue 6,
pp. 859-862,
06/01/1991
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M. Mueller, K. Wacker, W. F. Hickey, E. B. Ringelstein, and R. Kiefer Co-Localization of Multiple Antigens and Specific DNA : A Novel Method Using Methyl Methacrylate-Embedded Semithin Serial Sections and Catalyzed Reporter Deposition Am. J. Pathol., December 1, 2000; 157(6): 1829 - 1838. [Abstract] [Full Text] [PDF] |
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