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Rabbit anti-Human ARSB Polyclonal Antibody

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

ADC-27056A

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

$299.00

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Specifications


Cat.No ADC-27056A ClonalityPolyclonal
Host SpeciesRabbitTarget NameARSB
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthetic peptide of Human ARSBTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP15848
Background Information
  • Uniprot Id

    P15848

  • Target Species

    Human

  • Target Name

    ARSB

  • Target Full Name

    Arylsulfatase B

  • Target Function

    Removes sulfate groups from chondroitin-4-sulfate (C4S) and regulates its degradation. Involved in the regulation of cell adhesion, cell migration and invasion in colonic epithelium. In the central nervous system, is a regulator of neurite outgrowth and neuronal plasticity, acting through the control of sulfate glycosaminoglycans and neurocan levels.

  • Target Involvement

    Mucopolysaccharidosis 6 (MPS6); Multiple sulfatase deficiency (MSD)

  • Target Subcellular Location

    Lysosome. Cell surface.

  • Target Protein Families

    Sulfatase family

  • Target Research Area

    Cancer

  • Target Synonyms

    Arsb; ARSB_HUMAN; Arylsulfatase B; ArylsulfataseB; ASB; G4S; MPS6; N acetylgalactosamine 4 sulfatase; N-acetylgalactosamine-4-sulfatase

  • Target Background

    Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.

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