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Rabbit anti-Human GUSB Polyclonal Antibody

The antibody against GUSB was raised in rabbit using the Recombinant Human Beta-glucuronidase protein (382-651AA) 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-40104A

The antibody against GUSB was raised in rabbit using the Recombinant Human Beta-glucuronidase protein (382-651AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$299.00

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Specifications


Cat.No ADC-40104A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGUSB
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Beta-glucuronidase protein (382-651AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP08236
Background Information
  • Uniprot Id

    P08236

  • Target Species

    Human

  • Target Name

    GUSB

  • Target Full Name

    Beta-glucuronidase

  • Target Function

    Plays an important role in the degradation of dermatan and keratan sulfates.

  • Target Involvement

    Mucopolysaccharidosis 7 (MPS7)

  • Target Subcellular Location

    Lysosome.

  • Target Protein Families

    Glycosyl hydrolase 2 family

  • Target Synonyms

    Ac2-223; asd; Beta G1; Beta glucuronidase; Beta-G1; Beta-glucuronidase; BG; BGLR; BGLR_HUMAN; FLJ39445; Glucuronidase beta; Gur; Gus; Gus-r; Gus-s; Gus-t; Gus-u; GUSB; Gut; MPS7

  • Target Background

    This gene encodes a hydrolase that degrades glycosaminoglycans, including heparan sulfate, dermatan sulfate, and chondroitin-4, 6-sulfate. The enzyme forms a homotetramer that is localized to the lysosome. Mutations in this gene result in mucopolysaccharidosis type VII. Alternative splicing results in multiple transcript variants. There are many pseudogenes of this locus in the human genome.

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