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GAA Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 143671AP150UL

Description
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.Specifications
GAA | |
Polyclonal | |
Unconjugated | |
GAA | |
Acid maltase, Aglucosidase alfa, GAA, glucosidase, alpha; acid, LYAG, Lysosomal alpha glucosidase | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
14387, 2548, 367562 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot | |
0.16 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
P10253, P70699, Q6P7A9 | |
Gaa | |
GAA Fusion Protein Ag5690 | |
150 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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