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Contactin 4 antibody

CNTN4 Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7247339
  • Target See all Contactin 4 (CNTN4) Antibodies
    Contactin 4 (CNTN4)
    Reactivity
    Human, Mouse, Rat
    Host
    • 16
    • 3
    • 1
    • 1
    Rabbit
    Clonality
    • 18
    • 3
    Polyclonal
    Conjugate
    • 14
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Contactin 4 antibody is un-conjugated
    Application
    • 10
    • 7
    • 5
    • 4
    • 2
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogen
    Fusion protein of human CNTN4
    Isotype
    IgG
    Top Product
    Discover our top product CNTN4 Primary Antibody
  • Application Notes
    IHC 1:50-1:200, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.14 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Contactin 4 (CNTN4)
    Alternative Name
    CNTN4 (CNTN4 Products)
    Synonyms
    Axcam antibody, Big-2 antibody, AXCAM antibody, BIG-2 antibody, 9630050B05 antibody, FAR-1 antibody, MGC84491 antibody, zgc:153573 antibody, axcam antibody, big-2 antibody, cntn4a antibody, contactin 4 antibody, contactin 4 S homeolog antibody, Cntn4 antibody, CNTN4 antibody, cntn4.S antibody, cntn4 antibody
    Background
    This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.
    UniProt
    Q8IWV2
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