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Strumpellin anticorps (AA 380-530)

WASHC5 Reactivité: Humain WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7271349
  • Antigène Voir toutes Strumpellin (WASHC5) Anticorps
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Épitope
    • 3
    • 1
    • 1
    AA 380-530
    Reactivité
    • 4
    • 4
    • 2
    Humain
    Hôte
    • 5
    Lapin
    Clonalité
    • 5
    Polyclonal
    Conjugué
    • 5
    Cet anticorp Strumpellin est non-conjugé
    Application
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Fonction
    KIAA0196 Rabbit pAb
     Réactivité croisée
    Souris, Rat
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 380-530 of human KIAA0196 (NP_055661.3).
    Isotype
    IgG
  • Indications d'application
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Strumpellin (WASHC5) (WASH Complex Subunit 5 (WASHC5))
    Autre désignation
    KIAA0196 (WASHC5 Produits)
    Synonymes
    anticorps SPG8, anticorps AL022848, anticorps C76463, anticorps Kiaa0196, anticorps mKIAA0196, anticorps strumpellin, anticorps WASH complex subunit 5, anticorps WASHC5, anticorps washc5, anticorps Washc5
    Sujet
    This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease, a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.,RTSC, SPG8, RTSC1, KIAA0196,KIAA0196
    ID gène
    9897
    UniProt
    Q12768
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