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RCN2 anticorps

RCN2 Reactivité: Humain, Souris, Rat WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7011940
  • Antigène Voir toutes RCN2 Anticorps
    RCN2 (Reticulocalbin 2, EF-Hand Calcium Binding Domain (RCN2))
    Reactivité
    Humain, Souris, Rat
    Hôte
    • 10
    • 4
    Lapin
    Clonalité
    • 12
    • 2
    Polyclonal
    Conjugué
    • 14
    Cet anticorp RCN2 est non-conjugé
    Application
    • 13
    • 8
    • 5
    • 3
    • 3
    • 3
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human RCN2 (NP_002893.1).
    Isotype
    IgG
  • Indications d'application
    WB 1:500-1:2000 IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    RCN2 (Reticulocalbin 2, EF-Hand Calcium Binding Domain (RCN2))
    Autre désignation
    RCN2 (RCN2 Produits)
    Synonymes
    anticorps rcn2, anticorps MGC80678, anticorps si:dkey-24l11.6, anticorps zgc:110594, anticorps LOC733807, anticorps AA408742, anticorps Tcbp49, anticorps E6BP, anticorps ERC-55, anticorps ERC55, anticorps TCBP49, anticorps reticulocalbin 2 S homeolog, anticorps reticulocalbin 2, anticorps rcn2.S, anticorps RCN2, anticorps rcn2, anticorps Rcn2
    Sujet
    The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
    Poids moléculaire

    Observed_MW: 40 kDa

    Calculated_MW: 36 kDa/39 kDa

    ID gène
    5955
    UniProt
    Q14257
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