Xanthine Oxidase Enzyme for Uric Acid Metabolism Research >=5 U/mg 160 kDa Isoelectric Point 4.1 CAS 9002-17-9
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Xanthine Oxidase Enzyme for Uric Acid Metabolism Research >=5 U/mg 160 kDa Isoelectric Point 4.1 CAS 9002-17-9

Cat.No: IEC-HMM-0290 Datasheet

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Product Name Xanthine Oxidase Enzyme for Uric Acid Metabolism Research >=5 U/mg 160 kDa Isoelectric Point 4.1 CAS 9002-17-9
Catalog No. IEC-HMM-0290
Description Xanthine oxidase from Alta DiagnoTech catalyzes the oxidation of hypoxanthine to xanthine and xanthine to uric acid. It is used in purine metabolism research and as a component of analytical systems detecting xanthine-derived metabolites.
Intended Use Enzyme raw material for purine metabolism studies, uric acid research, and related diagnostic development.
Principle / Technology Oxidizes hypoxanthine and xanthine to uric acid with reduction of molecular oxygen to hydrogen peroxide or superoxide.
Detection Method Spectrophotometric, fluorometric, or amperometric H2O2 detection.
Sample Type Serum, plasma, research samples.
Performance Range / Specifications Specific activity >=5.0 U/mg. Molecular weight approximately 160 kDa. Isoelectric point 4.1.
Components / Formulation Xanthine oxidase lyophilized powder.
Storage Conditions -20°C.
Shelf Life Stable for at least 12 months at -20°C.
Package Specifications 1 g per bottle.
Product Form Brown amorphous powder.
Activity / Unit Definition >=5.0 U/mg
Molecular Weight Approximately 160 kDa
Source / Origin Microbial fermentation.
pH Range / Optimal pH Optimal pH 8.0; stable between pH 6.5-10.0 at 25°C for 20 hours.
Shipping Conditions Cold chain shipment.
Expiration Date / Stability -20°C stable for one year.
Appearance Brown amorphous powder.
CAS Number 9002-17-9
Isoelectric Point 4.1
Inhibitors Inhibited by Ag+, Hg2+, Cd2+, urea, cyanide, phosphate and chloride ions.
Optimal Temperature >45°C.
Thermal Stability Stable below 55°C.
Handling Precaution Stabilized by salicylate, cysteine, histamine and EDTA; handle with care to avoid oxidation.
Stabilizer Salicylate, cysteine, histamine and EDTA stabilize the enzyme.

For research use only, not for clinical use.

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