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.
70 kDa lysosomal alpha-glucosidase; 76 kDa lysosomal alpha-glucosidase; acid (Pompe disease, glycogen storage disease type II); acid alpha-glucosidase; Acid maltase; Acid maltase Aglucosidase alfa GAA glucosidase alpha acid LYAG Lysosomal alpha glucosidase; Aglucosidase alfa; glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II); Lysosomal alpha-glucosidase
Cat # 16832984
20 µL
Cat # 17176733
100 µg
Cat # 16148424
100 ug
Cat # 16822984
150 µL
Cat # 17239963
100 µg
Cat # 17286743
100 µL
Cat # 17159395
100 µL
Cat # 16559591
100 µL
Cat # 15914865
100 µg
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