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Invitrogen™ alpha Galactosidase Monoclonal Antibody (C8)
Mouse Monoclonal Antibody
Supplier: Invitrogen™ MA541589
This item is not returnable.
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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
alpha Galactosidase | |
Monoclonal | |
1 mg/mL | |
PBS with 50% glycerol and 0.05% ProClin 300 | |
P06280 | |
GLA | |
Recombinant protein Galactosidase Alpha. The antigen corresponds to amino acid range 81-429 of the target protein. | |
200 μL | |
Primary | |
Human | |
Antibody | |
IgG2b κ |
Immunohistochemistry (Paraffin), Western Blot | |
C8 | |
Unconjugated | |
GLA | |
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 | |
Mouse | |
Protein A/G | |
RUO | |
2717 | |
-20°C | |
Liquid |
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