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Invitrogen™ alpha Galactosidase Monoclonal Antibody (08)

Descripción
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.
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
Especificaciones
| Antígeno | alpha Galactosidase |
| Aplicaciones | ELISA |
| Clasificación | Monoclonal |
| Clon | 08 |
| Concentración | 1 mg/mL |
| Conjugado | Unconjugated |
| Formulación | PBS with no preservative |
| génica | GLA |
| N.º de referencia del gen | P06280 |
| Alias de gen | 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 |
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Título del producto
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