catalog number :
MBS747502
products type :
ELISA Kit
products full name :
Sheep alpha-Glucosidase ELISA Kit
products short name :
alpha-Glucosidase
products name syn :
Sheep a-Glucosidase ELISA Kit
other names :
alpha-glucosidase; Lysosomal alpha-glucosidase; lysosomal alpha-glucosidase; acid maltase; aglucosidase alfa; glucosidase, alpha; acid; Acid maltase; Aglucosidase alfaCleaved into the following 2 chains:76 kDa lysosomal alpha-glucosidase; 70 kDa lysosomal alpha-glucosidase
products gene name :
A-Glu
products gene name syn :
A-Glu
other gene names :
GAA; GAA; LYAG
uniprot entry name :
LYAG_HUMAN
storage stability :
Store all reagents at 2-8 degree C.
ncbi acc num :
ABI53718.1
ncbi mol weight :
105,324 Da
ncbi pathways :
Galactose Metabolism Pathway 82931!!Galactose Metabolism Pathway 292!!Lysosome Pathway 99052!!Lysosome Pathway 96865!!Metabolic Pathways 132956!!Notch-mediated HES/HEY Network Pathway 169347!!Starch And Sucrose Metabolism Pathway 82974!!Starch And Sucrose Metabolism Pathway 344
ncbi 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]