Anti-Alpha galactosidase A antibody

Catalog No : FT-FNab00328
294.00€
0.00€

Shipping cost plus VAT not included , delivery in 7-14 business days

Description 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.
Other names
Cellular localization
Research area Cardiovascular, Metabolism, Signal Transduction
Note This product is for research purpose only, not for use in diagnostics or as therapeutics.
Uniprot ID P06280
Product name Anti-Alpha galactosidase A antibody
Catalog No FT-FNab00328
Supplier’s Catalog No FNab00328
Supplier Fine Test (Wuhan Fine Biotech)
Host species Rabbit
Species reactivity Human, Mouse, Rat
Applications ELISA, IHC, IP, WB
Recommended dilutions WB: 1:500-1:5000, IHC: 1:20-1:200, IP: 1:500-1:5000
Molecular weight 49 kDa
Conjugate Unconjugated
Immunogen galactosidase, alpha
Specificity N/A
Storage Store at -20°C. Avoid repeated freeze and thaw cycles.
Clonality Polyclonal
Isotype IgG
Clone ID N/A
Concentration 1 mg/mL
Storage buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3
Formulation Liquid
Purification Immunogen affinity purified, ≥95% as determined by SDS-PAGE
Handling This product contains NaN3 as preservative, please take appropriate care when handling this product.
Reactivity life 12 months when stored properly according to instructions.