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GJC2 antibody (N-Term)

GJC2 Reactivity: Human WB Host: Mouse Monoclonal 391CT6-4-3 unconjugated
Catalog No. ABIN1538736
  • Target See all GJC2 Antibodies
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Binding Specificity
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 53-78, N-Term
    Reactivity
    • 19
    • 12
    • 11
    • 2
    • 1
    • 1
    Human
    Host
    • 17
    • 5
    Mouse
    Clonality
    • 17
    • 5
    Monoclonal
    Conjugate
    • 15
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This GJC2 antibody is un-conjugated
    Application
    • 15
    • 5
    • 4
    • 4
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    B, C, Ha, Zf, M, Pig, Rat, X
    Purification
    Mouse monoclonal antibody supplied in crude ascites with 0.09% (W/V) sodium azide.
    Immunogen
    This GJC2 antibody is generated from mice immunized with a KLH conjugated synthetic peptide between 53-78 amino acids from the N-terminal region of human GJC2.
    Clone
    391CT6-4-3
    Isotype
    IgM
    Top Product
    Discover our top product GJC2 Primary Antibody
  • Application Notes
    WB: 1:100~8000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Mouse monoclonal antibody supplied in crude ascites with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    GJC2 Antibody (N-term)(Ascites) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    Expiry Date
    6 months
  • Target
    GJC2 (Gap Junction Protein, gamma 2, 47kDa (GJC2))
    Alternative Name
    GJC2 (GJC2 Products)
    Background
    GJC2 is 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.
    Molecular Weight
    47002
    Gene ID
    57165
    NCBI Accession
    NP_065168
    UniProt
    Q5T442
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