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Rabbit anti-Human ARSA Polyclonal Antibody

The antibody against ARSA was raised in rabbit using the Recombinant Human Arylsulfatase A protein (208-507AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA.

ADC-44494A

The antibody against ARSA was raised in rabbit using the Recombinant Human Arylsulfatase A protein (208-507AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA.

$299.00

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Specifications


Cat.No ADC-44494A ClonalityPolyclonal
Host SpeciesRabbitTarget NameARSA
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISAStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Arylsulfatase A protein (208-507AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP15289
Background Information
  • Uniprot Id

    P15289

  • Target Species

    Human

  • Target Name

    ARSA

  • Target Full Name

    Arylsulfatase A

  • Target Function

    Hydrolyzes cerebroside sulfate.

  • Target Involvement

    Metachromatic leukodystrophy (MLD); Multiple sulfatase deficiency (MSD)

  • Target Subcellular Location

    Endoplasmic reticulum. Lysosome.

  • Target Protein Families

    Sulfatase family

  • Target Synonyms

    arsA; ARSA_HUMAN; arylsulfatase A; Arylsulfatase A component C; As 2; AS A; As2; ASA; AW212749; C230037L18Rik; Cerebroside-sulfatase; metachromatic leucodystrophy; MGC125207; MLD; OTTHUMP00000196546; OTTHUMP00000196548; TISP73

  • Target Background

    The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.

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