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Glucose Oxidase, A. niger

Cat no: G3052

Glucose Oxidase, A. niger

Since its discovery as an "antibiotic" (shown subsequently to be due to peroxide formation) there has been an interest in glucose oxidase, chiefly because of its utility in glucose estimation. For most clinical work the crude form of the A. niger enzyme has been satisfactory. However, it contains trace amount of polysaccharidases such as amylase, maltase and sucrase which can contribute to falsely high glucose levels. The purified enzyme is free of these traces and is recommended for analytical use in the presence of di-or polysaccharides. Glucose analytical systems employ the enzyme utilizing H2O2 production reacting with Fe(CN)-in the presence of luminol to produce luminescence proportional to the initial glucose concentration.\n\nComposition: The enzyme consists of two identical polypeptide chain subunits (80kD) covalently linked by disulfide bonds. Each subunit contains one mole of Fe and one mole of FAD (flavin-adenine dinucleotide). The molecule is approximately 74% protein, 16% neutral sugar and 2% amino sugars. FAD is replaceable with FHD (flavin-hypoxanthine dinucleotide) without loss of activity.\n\nSource: Aspergillus niger\n\nForm: Supplied as a dialyzed, lyophilized powder\n\nPurity: Chromatographically purified\n\nActivity: ~250u/mg (~300u/mg Protein)\n\nStorage and Stability: Stable for 12 months at 2-8 degrees C

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SPECIFICATIONS

Catalog Number

G3052

Size

100mg

Alternative Names

EC=1.1.3.4.

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