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Clinical Chemistry, Vol 18, 417-421, Copyright © 1972 by the American Association for Clinical Chemistry
1 Clinical Chemistry Section, Department of Clinical
Pathology, The University of Texas at Houston, M. D. Anderson
Hospital and Tumor Institute, Houston, Texas 77025.
We describe a new electrophoretic method for the
characterization of human serum and tissue alkaline phosphatases on cellulose acetate plates.
Enzymes are localized fluorometrically with the
substrate
-naphthol AS-MX phosphate or colorimetrically by coupling the reaction product with
Fast Blue RR. Both localization techniques are
sensitive enough to demonstrate isoenzyme patterns in micro-scale samples of normal sera. Our
electrophoretic studies indicate that sera of children and adults normally contain isoenzymes
originating from both liver and bone. The high sensitivity of the method allows the use of normal sera
as markers rather than tissue extracts, and isoenzyme patterns may be visually assessed after
heat inactivation and chemical inhibition. The
method is suitable for the electrophoretic fractionation of alkaline phosphatase in large numbers of
sera, with equipment and technique familiar to
many laboratories.
Submitted on December 22, 1971
Accepted on February 18, 1972
The following articles in journals at HighWire Press have cited this article:
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V. Abbassi, A.R. Colon, and R. H. Schwartz Benign Elevation of Serum Alkaline Phosphatase, Transient and Persistent Variety Clinical Pediatrics, June 1, 1984; 23(6): 336 - 337. [Abstract] [PDF] |
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