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2.
Clin Chem ; 34(9): 1857-62, 1988 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-3046780

RESUMEN

A modified agarose electrophoretic system for the separation of alkaline phosphatase (ALP, EC 3.1.3.1) isoenzymes is described. Bone, liver, high-molecular-mass, and intestinal ALP are separated with high reproducibility. The sensitivity of the agarose system is superior to cellulose acetate in detecting high-Mr ALP. Correlation is good between bone ALP fractions scanned before and after treatment with neuraminidase. Immunoglobulin-bound ALPs, the ALP-lipoprotein-X complex, and the additional ALP fraction observed in transient hyperphosphatasemia in children are detected by their peculiar electrophoretic mobility in the proposed system. Approximately 25% of the samples contained an additional fraction of intestinal-type ALP, as evidenced by neuraminidase treatment and use of polyclonal and monoclonal antibodies. Because the electrophoretic mobilities of this "intestinal variant" and of some immunoglobulin-bound ALP fractions are identical to those of bone and intestinal ALP, respectively, treatment of the samples with a polyclonal antibody that reacts with intestinal ALP is advised.


Asunto(s)
Fosfatasa Alcalina/sangre , Electroforesis en Gel de Agar , Electroforesis , Isoenzimas/sangre , Fosfatasa Alcalina/genética , Huesos/enzimología , Electroforesis en Acetato de Celulosa , Femenino , Variación Genética , Hepatitis B/enzimología , Humanos , Técnicas de Inmunoadsorción , Lactante , Intestinos/enzimología , Hígado/enzimología , Peso Molecular , Neuraminidasa/farmacología , Fosfatos/sangre , Placenta/enzimología
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