Anti-alpha Galactosidase A Mouse Monoclonal Antibody [clone: 2B2C5]

Supplier: Proteintech
66121-1-IG
10087-566EA 849.57 CAD
10087-566
Anti-alpha Galactosidase A Mouse Monoclonal Antibody [clone: 2B2C5]
Antibodies
GLA, also named as Melibiase, Agalsidas and Alpha-galactosidase A, Belongs to the glycosyl hydrolase 27 family. It hydrolysis of 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.

Western Blot: HeLa Cells, 1:500-1:5000; IHC: Human Kidney Tissue, 1:20-1:200; IF: HepG2 Cells, 1:20-1:200

Type: Primary
Antigen: [delete]
Clonality: Monoclonal
Clone: 2B2C5
Conjugation: Unconjugated
Epitope:
Host: Mouse
Isotype: IgG2a
Reactivity: Human
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