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Galactosidase alpha Rabbit anti-Human, Polyclonal, Bioss
SDP

Catalog No. 501987854
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50-198-7854 100 μL
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Catalog No. 50-198-7854 Supplier Bioss Supplier No. BS7593R
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Description

Rabbit Polyclonal Antibody

This gene 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.

Specifications

Antigen Galactosidase alpha
Applications Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Classification Polyclonal
Concentration 1 μg/mL
Conjugate Unconjugated
Formulation PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
Gene GLA
Gene Accession No. P06280
Gene Alias Agalsidase; agalsidase alfa; Ags; Alpha-D-galactosidase A; Alpha-D-galactoside galactohydrolase; alpha-D-galactoside galactohydrolase 1; alpha-gal A; Alpha-galactosidase A; GALA; galactosidase alpha; galactosidase, alpha; GLA; Melibiase
Gene Symbols GLA
Host Species Rabbit
Immunogen KLH conjugated synthetic peptide derived from human Galactosidase alpha.
Purification Method Protein A
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 2717
Target Species Human
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG
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