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Invitrogen™ alpha Galactosidase Polyclonal Antibody
Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA527349
This item is not returnable.
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Description
Recommended positive controls: 293T, HeLa, Rat Lung. Predicted reactivity: Rat (82%), Pig (84%), Bovine (80%). Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly 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 | |
| Polyclonal | |
| Unconjugated | |
| GLA | |
| Agalsidase; agalsidase alfa; Ags; Alpha-D-galactosidase A; alpha-D-galactoside galactohydrolase; alpha-D-galactoside galactohydrolase 1; alpha-gal A; alpha-galactosidase A; GALA; galactosidase alpha; galactosidase, alpha; GLA; Melibiase | |
| Rabbit | |
| Antigen affinity chromatography | |
| RUO | |
| 2717, 363494 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot | |
| 0.157 mg/mL | |
| PBS with 20% glycerol and 0.025% ProClin 300; pH 7 | |
| P06280 | |
| GLA | |
| Recombinant protein encompassing a sequence within the center region of human Galactosidase alpha. The exact sequence is proprietary. | |
| 100 μL | |
| Primary | |
| Human, Rat | |
| Antibody | |
| IgG |
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