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Product Description
anti- Alpha galactosidase A antibody is available at Gentaur for Next week Delivery.
Purification: Protein A+G purification
Background: GLA, also named as Melibiase, Agalsidase and Alpha-galactosidase A, belongs to the glycosyl hydrolase 27 family. It hydrolyzes terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy(ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease..
Immunogen: galactosidase, alpha
Synonyms: Alpha galactosidase A, galactosidase, alpha
Reactivity: Human
Tested Application: ELISA, WB, IHC, IF
Recommended dilution: WB: 1:500-1:2000; IHC: 1:20-1:200; IF: 1:20-1:200
Image 1: Immunohistochemistry of paraffin-embedded human kidney tissue slide using FNab00330(GLA Antibody) at dilution of 1:50
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Image 4: HeLa cells were subjected to SDS PAGE followed by western blot with FNab00330(GLA antibody) at dilution of 1:1000
Gene ID: 2717
Research Area: Metabolism
Uniprot ID: P06280
