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Rabbit anti-Human NAGA Polyclonal Antibody

The antibody against NAGA was raised in rabbit using the Human NAGA as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-52634A

The antibody against NAGA was raised in rabbit using the Human NAGA as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$600.00

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Specifications


Cat.No ADC-52634A ClonalityPolyclonal
Host SpeciesRabbitTarget NameNAGA
Target SynonymsNAGA antibody; Alpha-N-acetylgalactosaminidase antibody; EC 3.2.1.49 antibody; Alpha-galactosidase B antibodyFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.02% sodium azidePurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman NAGATarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP17050
Background Information
  • Uniprot Id

    P17050

  • Target Species

    Human

  • Target Name

    NAGA

  • Target Full Name

    Alpha-N-acetylgalactosaminidase

  • Target Function

    Removes terminal alpha-N-acetylgalactosamine residues from glycolipids and glycopeptides. Required for the breakdown of glycolipids.

  • Target Involvement

    Schindler disease (SCHIND); Kanzaki disease (KANZD)

  • Target Subcellular Location

    Lysosome.

  • Target Protein Families

    Glycosyl hydrolase 27 family

  • Target Synonyms

    NAGA; Alpha-N-acetylgalactosaminidase; EC 3.2.1.49; Alpha-galactosidase B

  • Target Background

    NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease).

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