Literature DB >> 2684138

Influence of fixation, exciting light and section thickness on the primary fluorescence of samples for microfluorometric analysis.

P Del Castillo1, A R Llorente, J C Stockert.   

Abstract

The primary fluorescence (autofluorescence) of some cell and tissue components depends on the fixative and fixing time, as well as on the thickness of paraffin sections and the wavelength of exciting light. The highest autofluorescence emission (pale green) was observed by using violet-blue excitation. After aldehyde fixation, the autofluorescence of some tissue structures was higher than after methanol or ethanolacetic acid. These features must be taken into account when fluorescence microscopy is applied to the study of cell smears and paraffin embedded tissues after flurochroming or immunofluorescence reactions.

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Mesh:

Year:  1989        PMID: 2684138

Source DB:  PubMed          Journal:  Basic Appl Histochem        ISSN: 0391-7258


  11 in total

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4.  Simple Elimination of Background Fluorescence in Formalin-Fixed Human Brain Tissue for Immunofluorescence Microscopy.

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7.  Selective fluorescence of eosinophilic structures in grasshopper and mammalian testis stained with haematoxylin-eosin.

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Authors:  J C Stockert; C I Trigoso; A R Llorente; P Del Castillo
Journal:  Histochem J       Date:  1991 Nov-Dec

9.  Characterizing and Diminishing Autofluorescence in Formalin-fixed Paraffin-embedded Human Respiratory Tissue.

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