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Connexin 31 antibody

GJB3 Reactivity: Human, Mouse, Rat IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2421455
  • Target See all Connexin 31 (GJB3) Antibodies
    Connexin 31 (GJB3) (Gap Junction Protein, beta 3, 31kDa (GJB3))
    Reactivity
    • 33
    • 13
    • 12
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 47
    • 1
    Rabbit
    Clonality
    • 46
    • 2
    Polyclonal
    Conjugate
    • 23
    • 11
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Connexin 31 antibody is un-conjugated
    Application
    • 37
    • 26
    • 20
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    Purification
    Antigen affinity purification
    Immunogen
    Recombinant protein of human GJB3
    Isotype
    IgG
    Top Product
    Discover our top product GJB3 Primary Antibody
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C/-80 °C
    Storage Comment
    Store at -20°C (regular) and -80°C (long term).
  • Target
    Connexin 31 (GJB3) (Gap Junction Protein, beta 3, 31kDa (GJB3))
    Alternative Name
    GJB3 (GJB3 Products)
    Synonyms
    CX31 antibody, DFNA2 antibody, DFNA2B antibody, EKV antibody, Cnx31 antibody, Cx31 antibody, D4Wsu144e antibody, Gjb-3 antibody, ekv antibody, cx31 antibody, dfna2 antibody, gjb3b antibody, dfna2b antibody, connexin-31 antibody, gap junction protein beta 3 antibody, gap junction protein, beta 3 antibody, gap junction protein beta 3 L homeolog antibody, GJB3 antibody, Gjb3 antibody, gjb3.L antibody, gjb3 antibody
    Background
    This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein.
    Synonyms: EKV, CX31, DFNA2, DFNA2B
    Pathways
    Sensory Perception of Sound
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