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Arylsulfatase A antibody

The Rabbit Polyclonal anti-Arylsulfatase A antibody has been validated for WB. It is suitable to detect Arylsulfatase A in samples from Human.
Catalog No. ABIN2854547

Quick Overview for Arylsulfatase A antibody (ABIN2854547)

Target

See all Arylsulfatase A (ARSA) Antibodies
Arylsulfatase A (ARSA)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Arylsulfatase A antibody is un-conjugated

Application

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Western Blotting (WB)
  • Cross-Reactivity

    Human

    Characteristics

    Rabbit Polyclonal antibody to Arylsulfatase A
    Arylsulfatase A antibody [N2C2], Internal

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein encompassing a sequence within the center region of human Arylsulfatase A. The exact sequence is proprietary.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: H1299 , HeLa

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.44 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    Arylsulfatase A (ARSA)

    Alternative Name

    arylsulfatase A

    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. Multiple alternatively spliced transcript variants, one of which encodes a distinct protein, have been described for this gene.

    Cellular Localization: Lysosome

    Molecular Weight

    54 kDa

    Gene ID

    410

    UniProt

    P15289
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