Extinction coefficient of polymerized diaminobenzidine complexed with cobalt as final reaction product of histochemical oxidase reactions
- 1 December 1995
- journal article
- Published by Springer Nature in Histochemistry and Cell Biology
- Vol. 104 (6) , 473-477
- https://doi.org/10.1007/bf01464338
Abstract
The extinction coefficient is essential for the conversion of cytophotometric (mean integrated) absorbance values into absolute units of enzyme activity, for instance expressed in terms of moles of substrate converted per unit time and per unit wet weight of tissue. The extinction coefficient of polymerized diaminobenzidine (polyDAB) complexed with cobalt as the final reaction product of oxidase reactions was estimated at 575 nm by comparison of the amounts of final reaction products formed after incubation of serial unfixed cryostat sections of rat kidney to demonstrate D-amino acid oxidase activity with either the tetrazolium salt method or the cerium-DAB-cobalt-hydrogen peroxide method. Both procedures resulted in similar localization patterns of final reaction product in a granular form in epithelial cells of proximal tubules in rat kidney. The granules were peroxisomes. Linear relationships were found for both methods between the specific amounts of final reaction product generated by D-amino acid oxidase activity and incubation time. The cerium salt method gave rise to 7.4 times higher absorbance values of final reaction product generated per unit time and per unit wet weight of tissue than the tetrazolium salt procedure. The extinction coefficient of tetranitro BT-formazan is 19 000 at 557 nm. Therefore, the cytophotometric extinction coefficient of the poly DAB-cobalt complex as final reaction product of oxidase reactions was established to be 140 000.Keywords
This publication has 15 references indexed in Scilit:
- A quantitative histochemical study of xanthine oxidase activity in rat liver using the cerium capture method in the presence of polyvinyl alcohol.Journal of Histochemistry & Cytochemistry, 1994
- Localization of uric acid oxidase activity in core and matrix of peroxisomes as detected in unfixed cryostat sections of rat liver.Journal of Histochemistry & Cytochemistry, 1994
- Cerium methods for light and electron microscopical histochemistryJournal of Microscopy, 1993
- The use of unfixed cryostat sections for electron microscopic study of D-amino acid oxidase activity in rat liver.Journal of Histochemistry & Cytochemistry, 1992
- Light microscopical detection of H2O2-generating oxidases using cerium ions and aqueous incubation mediaActa Histochemica, 1991
- Localization of xanthine oxidoreductase activity using the tissue protectant polyvinyl alcohol and final electron acceptor Tetranitro BT.Journal of Histochemistry & Cytochemistry, 1991
- A quantitative histochemical study of D-amino acid oxidase activity in rat liver in relationship with feeding conditions.Journal of Histochemistry & Cytochemistry, 1991
- Enhanced light microscopic visualization of oxidase activity with the cerium capture methodHistochemistry and Cell Biology, 1989
- Light microscopic visualization of the reaction product of cerium used for localization of peroxisomal oxidases.Journal of Histochemistry & Cytochemistry, 1988
- The out-of-range error in microdensitometryJournal of Molecular Histology, 1986