missing translation for 'onlineSavingsMsg'
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Descripción
Positive Samples: 293T, HepG2, DU145.
This gene encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.
Especificaciones
Especificaciones
| Antígeno | GAA |
| Aplicaciones | ELISA, Western Blot |
| Clasificación | Recombinant Monoclonal |
| Clon | 5L2L10 |
| Concentración | 0.8 mg/mL |
| Conjugado | Unconjugated |
| Formulación | PBS with 0.05% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3 |
| génica | Gaa |
| N.º de referencia del gen | P10253 |
| Alias de gen | 70 kDa lysosomal alpha-glucosidase; 76 kDa lysosomal alpha-glucosidase; acid (Pompe disease, glycogen storage disease type II); acid alpha-glucosidase; acid maltase; Aglucosidase alfa; E430018M07Rik; Gaa; glucosidase alpha, acid; glucosidase, alpha, acid; glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II); LYAG; Lysosomal alpha-glucosidase |
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Título del producto
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