Evaluation of nine different fixatives
- 1 January 1984
- journal article
- research article
- Published by Springer Nature in Histochemistry and Cell Biology
- Vol. 81 (3) , 213-219
- https://doi.org/10.1007/bf00495630
Abstract
An artificial substrate was developed for quantitative testing of the ability of various fixatives to preserve the reactivity of IgG and IgA isotypes (γ and α chains) and the secretory component (SC) of secretory IgA as model antigens. Polymerized normal rabbit serum was used as matrix and defined amounts (10–0.1 g/l) of antigen were incorporated into it by diffusion before fixation and paraffin embedding. The various fixatives comprised alcohol, routine formalin, glutaraldehyde(1%)-formalin, Baker's formol calcium, formol sublimate, acetic acid(2%)-formol saline, Bouin's fluid, Susa fixative, and carbodiimide. The detection sensitivity afforded by these fixatives was defined as the immunofluorescence staining end point. Compared to the reference value obtained with alcohol (γ and α chains, 0.06 g/l of IgG and IgA; SC, 0.12 g/l of colostral IgA), an antigen concentration at least 8 times higher was necessary for detection with most of the cross-linking fixatives. Bouin's and Susa fixatives were peculiar in that they required more than 150 times higher antigen concentration for detection of IgG but only 3–8 times higher for IgA. The determined sensitivities were compared with the immunofluorescence performance results obtained on human tissues prepared with the same fixatives; excepting carbodiimide (which produced unacceptable autofluorescence of the substrate matrix) a remarkably good correlation was found with regard to IgG- and IgA-producing cells (especially of the former isotype) and secretory epithelium (IgA and SC). However, the latter result depended on pronase treatment of the tissue sections to unmask epithelial antigens. It was concluded that detection sensitivity as determined with this artifical substrate may give a good idea about the immuno-histochemical performance obtained on tissue prepared with the actual fixative; but the degree of antigenic masking in the various tissue compartments has to be taken into account if the comparisons are to be meaningful.Keywords
This publication has 26 references indexed in Scilit:
- Evaluation of Nine Different Fixatives: 1. Preservation of Immunoglobulin Isotypes, J chain, and Secretory Component in Human TissuesPathology - Research and Practice, 1984
- Prolonged incubation time in immunohistochemistry: effects on fluorescence staining of immunoglobulins and epithelial components in ethanol- and formaldehyde-fixed paraffin-embedded tissues.Journal of Histochemistry & Cytochemistry, 1981
- Importance of fixation in immunohistochemistry: use of formaldehyde solutions at variable pH for the localization of tyrosine hydroxylase.Journal of Histochemistry & Cytochemistry, 1981
- Effects of fixation and processing on immunohistochemical demonstration of immunoglobulin in paraffin sections of tonsil and bone marrow.Journal of Clinical Pathology, 1980
- THE EFFECT OF FIXATION AND TRYPSINIZATION ON THE IMMUNOHISTOCHEMICAL DEMONSTRATION OF INTRACELLULAR IMMUNOGLOBULIN IN PARAFFIN EMBEDDED MATERIALActa Pathologica Microbiologica Scandinavica Section A Pathology, 1980
- Masking of protein antigen by modification of amino groups with carbobenzoxychloride (benzyl chloroformate) and demasking by treatment with nonspecific protease.Journal of Histochemistry & Cytochemistry, 1978
- Conjugates of Immunoglobulin G with Different FluorochromesScandinavian Journal of Immunology, 1973
- Human Secretory ImmunoglobulinsScandinavian Journal of Haematology, 1970
- The Cross-linking of Proteins with Glutaraldehyde and its use for the preparation of immunoadsorbentsImmunochemistry, 1969
- The reaction of glutaraldehyde with proteins and other biological materials*Journal of the Royal Microscopical Society, 1966