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Invitrogen™ alpha Galactosidase Monoclonal Antibody (C8)
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Catalog No. PIMA541589
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200 μL
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PIMA541589 200 μL
PIMA543975 20 μL
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Catalog No. PIMA541589 Supplier Invitrogen™ Supplier No. MA541589
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Mouse Monoclonal Antibody

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.
TRUSTED_SUSTAINABILITY

Specifications

Antigen alpha Galactosidase
Applications Immunohistochemistry (Paraffin), Western Blot
Classification Monoclonal
Clone C8
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.05% ProClin 300; 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 Mouse
Immunogen Recombinant protein Galactosidase Alpha. The antigen corresponds to amino acid range 81-429 of the target protein.
Purification Method Protein A/G
Quantity 200 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 2717
Target Species Human
Content And Storage Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Product Type Antibody
Form Liquid
Isotype IgG2b κ
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