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Arylsulfatase A anticorps

ARSA Reactivité: Humain, Souris ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7240571
  • Antigène Voir toutes Arylsulfatase A (ARSA) Anticorps
    Arylsulfatase A (ARSA)
    Reactivité
    • 56
    • 35
    • 34
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    Humain, Souris
    Hôte
    • 54
    • 16
    • 1
    Lapin
    Clonalité
    • 57
    • 14
    Polyclonal
    Conjugué
    • 35
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Arylsulfatase A est non-conjugé
    Application
    • 55
    • 21
    • 13
    • 13
    • 13
    • 10
    • 8
    • 7
    • 6
    • 4
    • 4
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human ARSA
    Isotype
    IgG
    Top Product
    Discover our top product ARSA Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.4 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Arylsulfatase A (ARSA)
    Autre désignation
    ARSA (ARSA Produits)
    Synonymes
    anticorps ARSA, anticorps zgc:101575, anticorps arsa, anticorps AS-A, anticorps ASA, anticorps AW212749, anticorps As-2, anticorps As2, anticorps TISP73, anticorps MLD, anticorps mld, anticorps arylsulfatase A, anticorps arylsulfatase, anticorps arylsulfatase A, gene 1 S homeolog, anticorps ARSA, anticorps arsa, anticorps arsA, anticorps RB6599, anticorps Arsa, anticorps arsa.1.S
    Sujet
    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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