LYAG

BT-AP03502

Rabbit

IgG

100ul,50ul,20ul

Polyclonal

Synthesized peptide derived from human LYAG

The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.221% sodium azide.

-20°C for 1 year

This gene encodes lysosomal alpha-glucosidase| which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. 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. Alternative splicing results in multiple transcript variants.

Human: P10253; Mouse: P70699; Rat: Q6P7A9;

Human: 2548; Mouse: 14387; Rat: 367562

LYAG; Lysosomal alpha-glucosidase; EC 3.2.1.20; Acid maltase; Aglucosidase alfa; 76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase;

Metabolism; Signal transduction

GAA