alpha-Galactosidase A/GLA Antibody (201) [Janelia Fluor® 549]

Sold under license from the Howard Hughes Medical Institute, Janelia Research Campus.

Galactosidase alpha encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. [provided by RefSeq]

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.

Array NBP2-90048JF549

• alpha-Galactosidase A/GLA Antibodies
• alpha-Galactosidase A/GLA Antibody Pair
• alpha-Galactosidase A/GLA ELISA Kits
• alpha-Galactosidase A/GLA Lysate
• alpha-Galactosidase A/GLA Proteins
• alpha-Galactosidase A/GLA Proteins and Enzyme