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Invitrogen™ alpha Galactosidase Polyclonal Antibody
Rabbit Polyclonal Antibody
Marca: Invitrogen™ PA513687
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Descripción
alpha Galactosidase Polyclonal Antibody for Western Blot, ICC/IF, IHC (P), Flow
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.
Especificaciones
| 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 | |
| Ammonium Sulfate Precipitation, Size-exclusion - Dialysis | |
| RUO | |
| 2717 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Flow Cytometry, Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry | |
| 2 mg/mL | |
| PBS with 0.09% sodium azide; pH 7.4 | |
| P06280 | |
| GLA | |
| KLH conjugated synthetic peptide between 83-112 amino acids from the N-terminal region of human GLA. | |
| 400 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
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