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Alpha galactosidase A Mouse anti-Human, Clone: 2B2C5, Proteintech
Mouse Monoclonal Antibody
Brand: Proteintech 66121-1-IG-150UL
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Description
This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predomitly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.Specifications
| Alpha galactosidase A | |
| Monoclonal | |
| 2.39 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| P06280 | |
| GLA | |
| Alpha galactosidase A Fusion Protein Ag7505 | |
| 150 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG2a |
| Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot | |
| 2B2C5 | |
| Unconjugated | |
| GLA | |
| Alpha galactosidase A, galactosidase, alpha | |
| Mouse | |
| Protein A | |
| RUO | |
| 2717 | |
| -20°C | |
| Liquid |
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Product Title
Alpha galactosidase A Mouse anti-Human, Clone: 2B2C5, Proteintech > 150 μL; Unconjugated
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