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Invitrogen™ alpha Galactosidase Recombinant Rabbit Monoclonal Antibody (30H11)
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Catalog No. FEMA550113
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FEMA550113 100 μL
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Catalog No. FEMA550113 Supplier Invitrogen™ Supplier No. MA550113
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Description

Rabbit Recombinant Monoclonal Antibody

alpha Galactosidase Recombinant Monoclonal Antibody for IHC (P), Flow, ELISA

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen alpha Galactosidase
Applications ELISA, Flow Cytometry, Immunohistochemistry (Paraffin)
Classification Recombinant Monoclonal
Clone 30H11
Concentration 1.23 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
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 A synthesized peptide derived from Human GLA.
Purification Method Affinity chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 2717
Target Species Human
Content And Storage -20°C or -80°C if preferred
Product Type Antibody
Form Liquid
Isotype IgG
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