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Rabbit anti-Human SGSH Polyclonal Antibody

The antibody against SGSH was raised in rabbit using the Recombinant Human N-sulphoglucosamine sulphohydrolase protein (273-502AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-40356A

The antibody against SGSH was raised in rabbit using the Recombinant Human N-sulphoglucosamine sulphohydrolase protein (273-502AA) 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-40356A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSGSH
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human N-sulphoglucosamine sulphohydrolase protein (273-502AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP51688
Background Information
  • Uniprot Id

    P51688

  • Target Species

    Human

  • Target Name

    SGSH

  • Target Full Name

    N-sulphoglucosamine sulphohydrolase

  • Target Function

    Catalyzes a step in lysosomal heparan sulfate degradation.

  • Target Involvement

    Mucopolysaccharidosis 3A (MPS3A)

  • Target Subcellular Location

    Lysosome.

  • Target Protein Families

    Sulfatase family

  • Target Synonyms

    Heparan sulfate sulfatase; Heparan sulphate sulphatase; HSS; MPS 3A; MPS3 A; MPS3A; Mucopolysaccharidosis type IIIA; N sulfoglucosamine sulfohydrolase (sulfamidase); N sulfoglucosamine sulfohydrolase; N-sulphoglucosamine sulphohydrolase; SFMD; SGSH; SPHM_HUMAN; Sulfoglucosamine sulfamidase; Sulphamidase; Sulphoglucosamine sulphamidase

  • Target Background

    This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.

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