Invitrogen™ alpha Galactosidase Monoclonal Antibody (C8)

Mouse Monoclonal Antibody

Catalog Number	Mfr. No.	Quantity
PIMA541589	Invitrogen™ MA541589	200 μL
PIMA543975	Invitrogen™ MA543975	20 μL

Description

alpha Galactosidase Monoclonal Antibody for Western Blot, IHC (P)

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: alpha Galactosidase
• Concentration: 1 mg/mL
• Applications: Immunohistochemistry (Paraffin), Western Blot
• Conjugate: Unconjugated
• Host Species: Mouse
• Regulatory Status: RUO
• Formulation: PBS with 50% glycerol and 0.05% ProClin 300
• Gene Accession No.: P06280
• Gene ID (Entrez): 2717
• Immunogen: Recombinant protein Galactosidase Alpha. The antigen corresponds to amino acid range 81-429 of the target protein.
• Product Type: Antibody

• Clone: C8
• Content And Storage: -20°C
• Classification: Monoclonal
• Form: Liquid
• Isotype: IgG2b κ
• Target Species: Human
• Gene: GLA
• 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
• Primary or Secondary: Primary
• Purification Method: Protein A/G