LYAG/GAA Antibody (3C6)

This product is produced by and distributed for Abnova, a company based in Taiwan.

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.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Showing Publications 1 - 2 of 2.

Publications using H00002548-M01	Applications	Species
Xiao J, Westbroek W, Motabar O et al. Discovery of a novel non-iminosugar acid alpha glucosidase chaperone series. J Med Chem. 2012-07-26 [PMID: 22834902]
Cheray M, Petit D, Forestier L et al. Glycosylation-related gene expression is linked to differentiation status in glioblastomas undifferentiated cells. Cancer Lett 2011-09-09 [PMID: 21899947]

Array H00002548-M01

• LYAG/GAA Antibodies
• LYAG/GAA ELISA Kits
• LYAG/GAA Kit
• LYAG/GAA Lysates
• LYAG/GAA Proteins
• LYAG/GAA Proteins and Enzymes