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Arylsulfatase E antibody (Middle Region)

ARSE Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1449829
  • Target See all Arylsulfatase E (ARSE) Antibodies
    Arylsulfatase E (ARSE)
    Binding Specificity
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    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)
    Sequence
    KVVHHDPPLL FDLSRDPSET HILTPASEPV FYQVMERVQQ AVWEHQRTLS
    Cross-Reactivity (Details)
    Species reactivity (tested):Human
    Purification
    Purified using peptide immunoaffinity column
    Immunogen
    Synthetic peptide directed towards the middle region of human ARSE
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    Discover our top product ARSE Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Reconstitution
    Add 50 μL of distilled water to a final concentration of 1 mg/mL.
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store lyophilized at 2-8 °C for one month or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
  • Target
    Arylsulfatase E (ARSE)
    Alternative Name
    Arylsulfatase E (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.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.Synonyms: ARSE, ASE
    Gene ID
    415
    NCBI Accession
    NP_000038
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