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Recombinant Human Arylsulfatase B (ARSB)

ACP08897

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP08897 Target NameARSB
Target SynonymsArsb; ARSB_HUMAN; Arylsulfatase B; ArylsulfataseB; ASB; G4S; MPS6; N acetylgalactosamine 4 sulfatase; N-acetylgalactosamine-4-sulfataseFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range37-533aa
Mol Weight72kDProtein LengthFull Length of Mature Protein
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot 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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