anti-Alpha galactosidase A antibody

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  • Alternative name

    Alpha galactosidase A, galactosidase, alpha antibody

  • Catalog
  • Size100μg
  • Formliquid
  • Purity≥95% as determined by SDS-PAGE
  • StoragePBS with 0.02% sodium azide and 50% glycerol pH 7.3 , -20℃ for 24 months (Avoid repeated freeze / thaw cycles.)
  • ClonalityPolyclonal Antibody
  • Host Rabbit
  • Species ReactivityHuman,Mouse ,Rat
  • Applications Tested/SuitableELISA,IHC,IP,WB
  • PurificationImmunogen affinity purified
  • Immunogengalactosidase, alpha
  • IHCImmunohistochemistry of paraffin-embedded human liver using A000328(GLA antibody) at dilution of 1:50
  • Western BlotHeLa cells were subjected to SDS PAGE followed by western blot with A000328(GLA antibody) at dilution of 1:1000
  • Recommended dilutionWB :1:500-1:5000;IHC:1:20-1:200;IP:1:500-1:5000
  • Product Description specificalGLA, 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.
  • Gene nameGLA
  • locationLysosome
  • Uniprot IDP06280
  • Calculated M.W.49kDa
  • Observed M.W.49 kDa

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