Galactosidase alpha Antibody / Gla

GLA is 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.

P06280

Rabbit

A portion of amino acids 83-112 from the human protein was used as the immunogen for the Galactosidase alpha antibody.

Polyclonal

Ig

FACS, IF, IHC-P, WB

Purified

In 1X PBS, pH 7.4, with 0.09% sodium azide

Aliquot the Galactosidase alpha antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

This Galactosidase alpha antibody is available for research use only.