Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

SLMAP anticorps

SLMAP Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6293579
  • Antigène Voir toutes SLMAP Anticorps
    SLMAP (Sarcolemma Associated Protein (SLMAP))
    Reactivité
    • 5
    • 2
    • 1
    Souris, Rat
    Hôte
    • 3
    • 2
    • 1
    • 1
    Lapin
    Clonalité
    • 5
    • 2
    Polyclonal
    Conjugué
    • 7
    Cet anticorp SLMAP est non-conjugé
    Application
    • 7
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human SLMAP
    Isotype
    IgG
    Top Product
    Discover our top product SLMAP Anticorps primaire
  • Indications d'application
    WB 1:500 - 1:2000
    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Antigène
    SLMAP (Sarcolemma Associated Protein (SLMAP))
    Autre désignation
    SLMAP (SLMAP Produits)
    Synonymes
    anticorps SLAP, anticorps D330001L02Rik, anticorps Slap, anticorps mKIAA1601, anticorps MGC55817, anticorps zgc:55817, anticorps SLMAP, anticorps fa03e05, anticorps fb39b03, anticorps wu:fa03e05, anticorps wu:fb39b03, anticorps zgc:153887, anticorps sarcolemma associated protein, anticorps sarcolemma associated protein b, anticorps sarcolemmal membrane-associated protein, anticorps sarcolemma associated protein a, anticorps SLMAP, anticorps Slmap, anticorps slmapb, anticorps slmap, anticorps LOC100435366, anticorps slmapa
    Sujet
    This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    95.198 kDa
    ID gène
    7871
    UniProt
    Q14BN4
Support technique