MAK129
β-Glucosidase Activity Assay Kit
sufficient for 100 colorimetric tests
Synonym(s):
Beta-Glucosidase Assay Kit
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About This Item
UNSPSC Code:
12161503
NACRES:
NA.84
usage
sufficient for 100 colorimetric tests
detection method
colorimetric
relevant disease(s)
neurological disorders; gastrointestinal diseases; hematological disorder
storage temp.
−20°C
Gene Information
human ... GBA(2629), GBA2(57704), GBA3(57733)
mouse ... GBA(14466), GBA2(230101)
rat ... GBA(684536), GBA2(298399), GBA3(289687)
Related Categories
General description
β-Glucosidase hydrolyzes carbohydrates by acting on terminal, non-reducing b(1→4)-linked D-glucose residues with the release of D-glucose. β-Glucosidases are required by organisms for the consumption of cellulose. Lysozyme, a β-glucosidase present in tears, acts on the β(1→4) glucose bonds present in the peptidoglycan cell wall of Gram-negative bacteria and helps to prevent bacterial infections in the eye. Defects in β-glucosidase activity have been implicated in Gaucher′s disease and Parkinson′s disease.
Application
β-Glucosidase Activity Assay Kit has been used to measure the β-glucosidase activity of the sample.
The β-Glucosidase Activity Assay kit provides a simple and direct procedure for measuring β-glucosidase activity in biological samples, for characterizing β-glucosidase production, and for the screening of β-glucosidase modulators.
Biochem/physiol Actions
In this assay, β-glucosidase activity is determined by a reaction in which β-glucosidase hydrolyzes p-nitrophenyl-β-D-glucopyranoside resulting in the formation of a colorimetric (405 nm) product, proportional to the β-glucosidase activity present. One unit of β-Glucosidse is the amount of enzyme that catalyzes the hydrolysis of 1.0 μmole substrate per minute at pH 7.0.
Features and Benefits
Compatible with high-throughput handling systems.
Storage Class
12 - Non Combustible Liquids
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Environmental Entomology, 44(6), 1531-1543 (2015)
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Recent metabolomic reports connect dysregulation of glycosphingolipids, particularly ceramide and glucosylceramide, to neurodegeneration and to motor unit dismantling in amyotrophic lateral sclerosis at late disease stage. We report here altered levels of gangliosides in the cerebrospinal fluid of amyotrophic lateral
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