anti-GAA antibody

Arigo Biolaboratories

anti-GAA antibody

23

Western Blot

Research Use Only

Polyclonal

Unconjugated

GAA

alpha glucosidase

acid maltase; aglucosidase alfa; glucosidase alpha, acid; LYAG; lysosomal alpha-glucosidase

Rabbit

IgG

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 Pompes 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. [provided by RefSeq, Jul 2008]

Human

-20°C

12352203