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Invitrogen™ alpha Galactosidase Monoclonal Antibody (2H7G10)

Mouse Monoclonal Antibody
Supplier: Invitrogen™ MA529309
Description
This product is preservative free. It is recommended to add sodium azide to avoid contamination (final concentration 0.05%-0.1%). This antibody has specificity for Human alpha-Galactosidase A/GLA.
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 | |
| Monoclonal | |
| 1 mg/mL | |
| PBS with no preservative | |
| P06280 | |
| GLA | |
| Recombinant Human alpha-Galactosidase A/GLA protein (Met1-Leu429). | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG2b |
| ELISA | |
| 2H7G10 | |
| 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 | |
| Mouse | |
| Protein A | |
| RUO | |
| 2717 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
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