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Arylsulfatase E antibody (Middle Region)

This Rabbit Polyclonal antibody specifically detects Arylsulfatase E in WB. It exhibits reactivity toward Human.
Catalog No. ABIN1449829

Quick Overview for Arylsulfatase E antibody (Middle Region) (ABIN1449829)

Target

See all Arylsulfatase E (ARSE) Antibodies
Arylsulfatase E (ARSE)

Reactivity

  • 20
  • 1
Human

Host

  • 20
  • 1
Rabbit

Clonality

  • 21
Polyclonal

Conjugate

  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Arylsulfatase E antibody is un-conjugated

Application

  • 9
  • 8
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    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
  • 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

    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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