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LiquiMAX Alcaline Phosphatase & #8211; SLR (méthode de l'IFCC / tampon AMP )

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Intended Use:
In vitro test for the quantitative determination of alkaline phosphatase (ALP) in human serum.

Product Features:
● Liquid Stable, Ready to use Mono Reagent
● Available as mono test vials
● PNPP Analogue used for better stability
● 2 Minutes increasing kinetic reaction (60Sec Delay+60 Sec
Measuring)
● Measuring Wavelength 405 nm
● Kinetic factor 3750 at 37° C.
● Linearity 1250 IU/L
● Serum is the only specimen
● Available as multipurpose reagents and dedicated system packs

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Désignation des marsandises

Alkaline phosphatase in serum consists of four structural genotypes: the liver-bone-kidney type, the intestinal type, the placental type and the variant from germ cells. It occurs in osteoblasts, hepatocytes, kidneys, spleen, placenta, prostate, leukocytes and the small intestine. The liverbone-kidney type is particularly important. A rise in the Alkaline Phosphatase activity occurs with all forms of cholestasis, particularly with obstructive jaundice. It is also elevated in diseases of the skeletal system, such as Paget`s disease, hyperparathyroidism, rickets and osteomalacia, as well as with fractures and malignant tumors. A considerable rise in the Alkaline Phosphatase activity is sometimes seen in children and juveniles. It is caused by increased osteoblast activity following accelerated bone growth. Various reference values for the purposes of clinical evaluation have been assigned to differing age groups. In 1946, Bessey, Lowry and Brock published a method for the determination of Alkaline Phosphatase using p-nitrophenyl phosphate as substrate buffered with glycine/NaOH. This assay described here meets the IFCC recommendations and uses AMPbuffer.

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  • Store Name: Avecon Healthcare
  • Vendor: Avecon Healthcare
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