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Rabbit anti-Human Galactosidase alpha (GLA) Monoclonal Antibody

The antibody against Galactosidase alpha (GLA) was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 50-150 of human Galactosidase alpha (GLA) (GLA) (P06280) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-13939A

The antibody against Galactosidase alpha (GLA) was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 50-150 of human Galactosidase alpha (GLA) (GLA) (P06280) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-13939A ClonalityMonoclonal
Host SpeciesRabbitTarget NameGalactosidase alpha (GLA)
Target SynonymsGALA; Galactosidase alpha (GLA)FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesRat brain, Mouse brain, RajiApplicationELISA, WB

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 50-150 of human Galactosidase alpha (GLA) (GLA) (P06280).Target SpeciesHuman
Immunogen SequenceFMCNLDCQEEPDSCISEKLFMEMAELMVSEGWKDAGYEYLCIDDCWMAPQRDSEGRLQADPQRFPHGIRQLANYVHSKGLKLGIYADVGNKTCAGFPGSFGUniprot IDP06280
Background Information
  • Uniprot Id

    P06280

  • Target Species

    Human

  • Target Name

    GLA

  • Target Full Name

    Alpha-galactosidase A

  • Target Function

    Catalyzes the hydrolysis of glycosphingolipids and participates in their degradation in the lysosome.

  • Target Involvement

    Fabry disease (FD)

  • Target Subcellular Location

    Lysosome.

  • Target Protein Families

    Glycosyl hydrolase 27 family

  • Target Research Area

    Cardiovascular

  • Target Synonyms

    AGAL_HUMAN; 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

  • Target Background

    This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

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