MAK123
α-Glucosidase Activity Assay Kit
sufficient for 100 colorimetric tests
Synonym(s):
α-Glucosidase Test Kit
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About This Item
NACRES:
NA.84
UNSPSC Code:
12161503
usage
sufficient for 100 colorimetric tests
detection method
colorimetric
relevant disease(s)
endocrinological disorders, diabetes; neurological disorders
storage temp.
−20°C
Gene Information
human ... GAA(2548)
mouse ... GAA(14387)
rat ... GAA(367562)
Related Categories
General description
α-Glucosidase hydrolyzes carbohydrates by acting on terminal, non-reducing a(1→4)-linked D-glucose residues with the release of D-glucose. Defects in α-glucosidase have been implicated in Pompe disease and diabetes.
Application
α-Glucosidase Activity Assay Kit has been used to measure the activity of a-glucosidase.
Suitable for the detection of α-glucosidase activity in biological samples.
Biochem/physiol Actions
In this assay,α-glucosidase activity is determined by a reaction in which α-glucosidase hydrolyzes p-nitrophenyl-α-D-glucopyranoside resulting in the formation of a colorimetric (405 nm) product, proportional to the α-glucosidase activity present
Features and Benefits
Compatible with high-throughput handling systems.
Storage Class
10 - Combustible liquids
wgk
WGK 2
Regulatory Information
监管及禁止进口产品
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Epigallocatechin gallate affects glucose metabolism and increases fitness and lifespan in Drosophila melanogaster.
Wagner A E, et al.
Oncotarget, 6(31), 30568-30568 (2015)
Anika E Wagner et al.
Oncotarget, 6(31), 30568-30578 (2015-09-17)
In this study, we tested whether a standardized epigallocatechin-3-gallate (EGCG) rich green tea extract (comprising > 90% EGCG) affects fitness and lifespan as well as parameters of glucose metabolism and energy homeostasis in the fruit fly, Drosophila melanogaster. Following the
Inhibitory effect of rhubarb on intestinal a-glucosidase activity in type 1 diabetic rats.
Hou K J, et al.
Tropical Journal of Pharmaceutical Research, 16(6), 1293-1297 (2017)
Atta-ur-Rahman.
Studies in Natural Products Chemistry, Volume 37 (2017)
Structure of human lysosomal acid a-glucosidase?a guide for the treatment of Pompe disease.
Veronique R Z, et al.
Nature Communications, 8(1), 1111-1111 (2017)
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