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Arylsulfatase E antibody

ARSE Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN636061
  • Target See all Arylsulfatase E (ARSE) Antibodies
    Arylsulfatase E (ARSE)
    Reactivity
    Human
    Host
    • 17
    • 1
    Rabbit
    Clonality
    • 18
    Polyclonal
    Conjugate
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Arylsulfatase E antibody is un-conjugated
    Application
    • 7
    • 7
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purified
    Immunogen
    ARSE antibody was raised using a synthetic peptide corresponding to a region with amino acids KVVHHDPPLLFDLSRDPSETHILTPASEPVFYQVMERVQQAVWEHQRTLS
    Top Product
    Discover our top product ARSE Primary Antibody
  • Application Notes
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Comment

    ARSE Blocking Peptide, catalog no. 33R-4727, is also available for use as a blocking control in assays to test for specificity of this ARSE antibody

    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ARSE antibody in PBS
    Concentration
    Lot specific
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target
    Arylsulfatase E (ARSE)
    Alternative Name
    ARSE (ARSE Products)
    Synonyms
    ASE antibody, CDPX antibody, CDPX1 antibody, CDPXR antibody, ARSE antibody, MGC155058 antibody, arylsulfatase E (chondrodysplasia punctata 1) antibody, arylsulfatase E antibody, ARSE antibody, Arse antibody
    Background
    Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene.
    Molecular Weight
    62 kDa (MW of target protein)
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