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GJC2 anticorps

GJC2 Reactivité: Humain, Souris, Rat ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2425719
  • Antigène Voir toutes GJC2 Anticorps
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Reactivité
    • 21
    • 13
    • 11
    • 2
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 17
    • 6
    Lapin
    Clonalité
    • 17
    • 6
    Polyclonal
    Conjugué
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GJC2 est non-conjugé
    Application
    • 16
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human GJC2
    Isotype
    IgG
    Top Product
    Discover our top product GJC2 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Autre désignation
    Connexin 47 (GJC2 Produits)
    Synonymes
    anticorps GJA12, anticorps cx47, anticorps gja12, anticorps cx46.6, anticorps pmldar, anticorps MGC146420, anticorps B230382L12Rik, anticorps Cx47, anticorps Gja12, anticorps CX46.6, anticorps HLD2, anticorps LMPH1C, anticorps PMLDAR, anticorps SPG44, anticorps gap junction protein gamma 2, anticorps si:dkey-91f15.1, anticorps gap junction protein, gamma 2, anticorps GJC2, anticorps gjc2, anticorps si:dkey-91f15.1, anticorps Gjc2
    Sujet
    This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1.
    NCBI Accession
    NP_065168
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