Alpha galactosidase A Monoclonal Antibody

  • monoclonal antibody-Elabscience
  • monoclonal antibody-Elabscience
  • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
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    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience
    • monoclonal antibody-Elabscience

      Catalog number:E-AB-27019

      Synonyms:AGAL,Agalsidase alfa,Alpha D galactosidase A,Alpha D galactoside galactohydrolase 1,Alpha D galactoside galactohydrolase,Alpha gal A,Alpha galactosidase A,Alpha-D-galactosidase A,Alpha-D-galactoside galactohydrolase,Alpha-galactosidase A,GALA,Galactosidase,alpha,GLA,GLA protein,Melibiase

      Size:
      • 60μL
      • 120μL
      • 200μL
      Qty:
      - +
      Price: $185

      Host: Mouse

      Reactivity: H

      Applications: WB,IHC,IF,ELISA

      Lead Time: 7~10 daysWelcome to order from local distributors.

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      Overview

      Synonyms AGAL,Agalsidase alfa,Alpha D galactosidase A,Alpha D galactoside galactohydrolase 1,Alpha D galactoside galactohydrolase,Alpha gal A,Alpha galactosidase A,Alpha-D-galactosidase A,Alpha-D-galactoside galactohydrolase,Alpha-galactosidase A,GALA,Galactosidase,alpha,GLA,GLA protein,Melibiase
      Swissprot P06280
      Source Mouse
      Reactivity Human
      Immunogen Fusion protein of Alpha galactosidase A
      Application WB,IHC,IF,ELISA
      Recommended dilution WB 1:500-1:5000, IHC 1:20-1:200, IF 1:20-1:200
      Clonality Monoclonal

      Properties

      Clone No Clone:407
      Isotype IgG2a
      Purification Protein A purification
      Conjugation Unconjugated
      Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
      Storage buffer PBS with 0.02% sodium azide, 50% glycerol, PH7.3
      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.

      Images

      Western Blot analysis of HeLa cells using Alpha galactosidase A Monoclonal Antibody at dilution of 1:1000

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