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Arylsulfatase A antibody

ARSA Reactivity: Human, Mouse, Rat WB, FACS Host: Mouse Monoclonal 4C10 unconjugated
Catalog No. ABIN6654013
  • Target See all Arylsulfatase A (ARSA) Antibodies
    Arylsulfatase A (ARSA)
    Reactivity
    • 39
    • 32
    • 31
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 44
    • 8
    • 1
    Mouse
    Clonality
    • 47
    • 6
    Monoclonal
    Conjugate
    • 27
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Arylsulfatase A antibody is un-conjugated
    Application
    • 37
    • 13
    • 12
    • 12
    • 10
    • 10
    • 7
    • 7
    • 6
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Flow Cytometry (FACS)
    Purification
    Protein G affinity
    Immunogen
    Amino acids QALKQLQLLKAQLDAAVTFGPSQVARGED were used as the immunogen for the ARSA antibody.
    Clone
    4C10
    Isotype
    IgG2a
    Top Product
    Discover our top product ARSA Primary Antibody
  • Application Notes
    Optimal dilution of the ARSA antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,Flow Cytometry: 1-3 μg/10^6 cells
    Restrictions
    For Research Use only
  • Buffer
    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
    Storage
    -20 °C
    Storage Comment
    After reconstitution, the ARSA antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target
    Arylsulfatase A (ARSA)
    Alternative Name
    ARSA (ARSA Products)
    Background
    Arylsulfatase A (ARSA) is an enzyme that breaks down sulfatides, namely cerebroside 3-sulfate intocerebroside and sulfate. In humans, arylsulfatase A is encoded by the ARSA gene. ARSA is mapped to 22q13.33. 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.
    UniProt
    P15289
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