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Anti-GLA antibody produced in rabbit Ab1, Prestige Antibodies(R) Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

ITEM#: 3042-HPA00023725UL

MFR#: HPA000237-25UL

alpha-D-Galactosidase A (GLA), a lysosomal enzyme, is a glycoside hydrolase that removes alpha-galactosyl moieties from glycolipid and glycoprotein glycans. Lack of GLA results in the accumulation of globotriaosylsphingosine (Gb3) in a variety of tis

alpha-D-Galactosidase A (GLA), a lysosomal enzyme, is a glycoside hydrolase that removes alpha-galactosyl moieties from glycolipid and glycoprotein glycans. Lack of GLA results in the accumulation of globotriaosylsphingosine (Gb3) in a variety of tissues resulting in the pathology called Fabry disease (FD).