Plateau absorbance measurements: An alternative approach to enzyme activity determination illustrated by the example of alkaline phosphatase
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Anatomy
Link
http://link.springer.com/content/pdf/10.1007/BF01753363.pdf
Reference18 articles.
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2. GEERTS, A. & ROELS, F. (1981) Quantitation of catalase activity by microspectrophotometry after diaminobenzidine staining.Histochemistry 72, 357–67.
3. GORDON, M. & ROBERTSON, W. R. (1986) The application of continuous monitoring microdensitometry to an analysis of NAD+ binding and 3β-hydroxy-Δ5-steroid dehydrogenase activity in the regressing corpus luteum of the pro-oestrous rat ovary.Histochem J. 18, 41–4.
4. KUGLER, P. (1981) Kinetic and morphometric measurements of enzyme reactions in tissue sections with a new instrumental setup.Histochemistry 71, 433–49.
5. MEIJER, A. E. F. H. & VLOEDMAN, A. H. T. (1984) Diazonium inactivation in simultaneous-coupling and product inhibition in post-coupling azo-techniques for demonstrating activity of acid hydrolases.Histochemistry 80, 187–92.
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1. Demonstration of 5′-nucleotidase activity in unfixed cryostat sections of rat liver using a combined light- and electron-microscope procedure;The Histochemical Journal;1995-11
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3. A novel fluorescence detection method for in situ hybridization, based on the alkaline phosphatase-fast red reaction.;Journal of Histochemistry & Cytochemistry;1992-09
4. An in situ hybridization histochemistry method for the use of alkaline phosphatase-labeled oligonucleotide probes in small intestine.;Journal of Histochemistry & Cytochemistry;1991-10
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