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Rabbit anti-Human GAA Polyclonal Antibody

The antibody against GAA was raised in rabbit using the Recombinant Human Lysosomal alpha-glucosidase protein (601-952AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.

ADC-16014A

The antibody against GAA was raised in rabbit using the Recombinant Human Lysosomal alpha-glucosidase protein (601-952AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC, IF.

$299.00

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Specifications


Cat.No ADC-16014A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGAA
FormLiquidSpecies ReactivityHuman, Mouse
IsotypeIgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification Method>95%, Protein G purifiedConjugateNon-conjugated
ApplicationELISA, IF, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Lysosomal alpha-glucosidase protein (601-952AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP10253
Background Information
  • Uniprot Id

    P10253

  • Target Species

    Human

  • Target Name

    GAA

  • Target Full Name

    Lysosomal alpha-glucosidase

  • Target Function

    Essential for the degradation of glycogen in lysosomes. Has highest activity on alpha-1,4-linked glycosidic linkages, but can also hydrolyze alpha-1,6-linked glucans.

  • Target Involvement

    Glycogen storage disease 2 (GSD2)

  • Target Subcellular Location

    Lysosome. Lysosome membrane.

  • Target Protein Families

    Glycosyl hydrolase 31 family

  • Target Synonyms

    70 kDa lysosomal alpha-glucosidase; Acid alpha glucosidase; Acid maltase; Aglucosidase alfa; Alpha glucosidase; GAA; Glucosidase alpha acid (Pompe disease glycogen storage disease type II); Glucosidase alpha acid; Glucosidase alpha; LYAG; LYAG_HUMAN; Lysosomal alpha glucosidase

  • Target Background

    This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants.

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