Galactosidase Alpha (GLA) Antibody

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.
Supplier Abbexa Ltd.
Product # abx032961-80UL
Pricing 80 µl USD $290.0
Clonality Polyclonal
Conjugation Unconjugated
Host Rabbit
Tested Applications ELISA, WB, IHC, IF/ICC, FCM
UniProt Primary AC P06280
Dry Ice No
Availability Shipped within 5-10 working days.
Note This product is for research use only.
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