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GJC2 antibody

GJC2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN3016915
  • Target See all GJC2 Antibodies
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Reactivity
    • 21
    • 13
    • 11
    • 2
    • 1
    • 1
    Human
    Host
    • 17
    • 6
    Rabbit
    Clonality
    • 17
    • 6
    Polyclonal
    Conjugate
    • 16
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GJC2 antibody is un-conjugated
    Application
    • 16
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human GJC2
    Isotype
    IgG
    Top Product
    Discover our top product GJC2 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Alternative Name
    GJC2 (GJC2 Products)
    Synonyms
    GJA12 antibody, cx47 antibody, gja12 antibody, cx46.6 antibody, pmldar antibody, MGC146420 antibody, B230382L12Rik antibody, Cx47 antibody, Gja12 antibody, CX46.6 antibody, HLD2 antibody, LMPH1C antibody, PMLDAR antibody, SPG44 antibody, gap junction protein gamma 2 antibody, si:dkey-91f15.1 antibody, gap junction protein, gamma 2 antibody, GJC2 antibody, gjc2 antibody, si:dkey-91f15.1 antibody, Gjc2 antibody
    Background
    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.,GJC2,CX46.6,Cx47,GJA12,HLD2,LMPH1C,PMLDAR,SPG44,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Gap Junctions,Cytoskeleton,Neuroscience,GJC2
    Molecular Weight
    47 kDa
    Gene ID
    57165
    UniProt
    Q5T442
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