Product Description
| Cat Number | E-BC-K821-M_96T |
|---|---|
| Category | Cell Metabolism Assay Kit |
| Pack Size | 96T |
| Detection Method | Colorimetric method |
| Research Field | Glycolysis and Lipid Metabolism |
| Sensitivity | 0.35 U/L |
| Detection Range | 0.35-33.43 U/L |
| Sample Type | tissue;fungus |
| Assay Length | 50 min |
| Target Synonyms | α-GC |
| Reader | Microplate reader |
| Test Principle | α-Glucosidase (α-GC), also known as α-D-glucoside hydrolase, is widely distributed in nature, with a wide variety of species and different properties, and exists in almost all organisms. It has important physiological functions in carbohydrate metabolism in animals, plants and microorganisms. If α-GC is deficient, it leads to severe glycogen metabolism disorders and excessive glycogen accumulation, which can cause Pompah's disease (an autosomal recessive inherited glycogen storage disease, also known as glycogenosis type II). Long-term low α-GC activity in human tissues can cause muscle fiber destruction and muscle atrophy. The detection principle of this kit is that the chromogenic substance generated by the substrate reaction catalyzed by α-glucosidase has the maximum absorption at 400 nm, and the enzyme activity of α-GC can be reflected by measuring its OD value at 400 nm. |
| Storage | This product can be stored at 2~8°C/-20°C~-80°C for 12 months with shading light. Please refer to the manual for the specific storage condition of the components. |
| Technical Manual | View Document |
| Msds | View Document |
| Product Url | View Document |
| Note | The product is for research use only |
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