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Alpha galactosidase A Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech Non-distribution product as customer accommodation.

Rabbit Polyclonal Antibody

Manufacturer:  Proteintech Group IncSupplier Diversity Partner 154281AP

Catalog No. 50-173-0221


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Description

Description

This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predomitly 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.
Specifications

Specifications

Alpha galactosidase A
0.16 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
P06280, P51569
Alpha galactosidase A, galactosidase, alpha
Rabbit
IgG
150 μL
-20°C
Primary
11605, 2717, 363494
Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot
Unconjugated
GLA
Liquid
GLA
Alpha galactosidase A Fusion Protein Ag7609
Antigen Affinity Chromatography
RUO
Antibody
Polyclonal
Human, Mouse, Rat
Documents
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