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About This Item
NACRES:
NA.84
UNSPSC Code:
12352200
usage
sufficient for 100 fluorometric tests
detection method
fluorometric
storage temp.
−20°C
General description
Phosphate is an essential component in living organisms and contributes to a variety of biological functions, including structural roles within nucleic acids, cellular membranes and bone. Phosphate is also important in the transport of cellular energy, nucleic acid metabolism and signal transduction. Hyperphosphatemia, a condition of excess phosphate levels in the blood, can lead to calcification of organs and interference with usage of other inorganic ions, such as iron, calcium, magnesium and zinc.
Application
Suitable for the detection of inorganic phosphate (Pi) produced through reactions involving ATPases, GTPases, 5′-nucleotidase, protein phosphatases, acidand alkaline phosphatases, phosphorylase, etc. from a variety of samples
Biochem/physiol Actions
The Phosphate Fluorometric Assay Kit provides a simple and direct procedure for measuring phosphate in a variety of samples. Phosphate reacts with maltose to produce glucose in the presence of an enzyme. The glucose is subsequently oxidized and reacts with a probe, resulting in a fluorometric (λex = 535/λem = 587 nm) product proportional to the amount of phosphate present. This kit has a linear range of detection between 50-250 pmoles.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Resp. Sens. 1
Storage Class
10 - Combustible liquids
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
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Fluid, Electrolyte and Acid-Base Disorders (2014)
Advanced Biology for you. (2000)
Serum phosphate levels and mortality risk among people with chronic kidney disease.
Kestenbaum B, et al.
Journal of the American Society of Nephrology, 16(2), 520-528 (2005)
Biochemical, Physiological, and Molecular Aspects of Human Nutrition-E-Book (2013)
Sara D Siegel et al.
mBio, 10(1) (2019-02-21)
The widely conserved LytR-CpsA-Psr (LCP) family of enzymes in Gram-positive bacteria is known to attach glycopolymers, including wall teichoic acid, to the cell envelope. However, it is undetermined if these enzymes are capable of catalyzing glycan attachment to surface proteins.
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