GAA
glucosidase, alpha; acid
LYAG
Human GAA (2548), Mouse Gaa (14387), Rat Gaa (367562), Zebrafish gaa (100002366), chicken GAA (416462), dog GAA (483352), domestic cat GAA (101086359), cow GAA (280798), Horse GAA (100056675), sheep GAA (101121692) ...More
- Human(2548) Summary: 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. [provided by RefSeq, Jul 2008]
- Mouse(14387) glucosidase, alpha, acid
- Rat(367562) glucosidase, alpha, acid
- Zebrafish(100002366) glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II)
- chicken(416462) glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II)
- dog(483352) glucosidase, alpha; acid
- domestic cat(101086359) glucosidase, alpha; acid
- cow(280798) glucosidase, alpha; acid
- Horse(100056675) glucosidase, alpha; acid
- sheep(101121692) glucosidase, alpha; acid
- naked mole-rat(101718861) glucosidase, alpha; acid
- domestic guinea pig(100728030) glucosidase, alpha; acid
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Antibodies
Monoclonal Anti-GAA antibody produced in mouse, clone 3C6, purified immunoglobulin, buffered aqueous solution,
human
ELISA
western blot
western blot
Anti-GAA antibody produced in rabbit, affinity isolated antibody,
bovine, dog, guinea pig, human, mouse, rat
immunohistochemistry
western blot
western blot
Anti-GAA antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunohistochemistry
western blot
western blot
Anti-GAA antibody produced in mouse, purified immunoglobulin, buffered aqueous solution,
human
western blot