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Arylsulfatase E anticorps

ARSE Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN636061
  • Antigène Voir toutes Arylsulfatase E (ARSE) Anticorps
    Arylsulfatase E (ARSE)
    Reactivité
    Humain
    Hôte
    • 17
    • 1
    Lapin
    Clonalité
    • 18
    Polyclonal
    Conjugué
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Arylsulfatase E est non-conjugé
    Application
    • 7
    • 7
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB)
    Purification
    Affinity purified
    Immunogène
    ARSE antibody was raised using a synthetic peptide corresponding to a region with amino acids KVVHHDPPLLFDLSRDPSETHILTPASEPVFYQVMERVQQAVWEHQRTLS
    Top Product
    Discover our top product ARSE Anticorps primaire
  • Indications d'application
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    Commentaires

    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
    Conseil sur la manipulation
    Avoid repeated freeze/thaw cycles.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène
    Arylsulfatase E (ARSE)
    Autre désignation
    ARSE (ARSE Produits)
    Synonymes
    anticorps ASE, anticorps CDPX, anticorps CDPX1, anticorps CDPXR, anticorps ARSE, anticorps MGC155058, anticorps arylsulfatase E (chondrodysplasia punctata 1), anticorps arylsulfatase E, anticorps ARSE, anticorps Arse
    Sujet
    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.
    Poids moléculaire
    62 kDa (MW of target protein)
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