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NOTCH3 antibody

NOTCH3 Reactivity: Human, Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257108
  • Target See all NOTCH3 Antibodies
    NOTCH3 (Notch 3 (NOTCH3))
    Reactivity
    • 49
    • 16
    • 10
    • 1
    Human, Mouse, Rat
    Host
    • 33
    • 16
    • 3
    • 1
    • 1
    Rabbit
    Clonality
    • 37
    • 18
    Polyclonal
    Conjugate
    • 29
    • 5
    • 4
    • 4
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NOTCH3 antibody is un-conjugated
    Application
    • 27
    • 25
    • 21
    • 10
    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    A synthetic peptide of human NOTCH3 (NP_000426.2).
    Isotype
    IgG
    Top Product
    Discover our top product NOTCH3 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    NOTCH3 (Notch 3 (NOTCH3))
    Alternative Name
    NOTCH3 (NOTCH3 Products)
    Synonyms
    CADASIL antibody, CASIL antibody, IMF2 antibody, AW229011 antibody, N3 antibody, hpbk antibody, fa14b08 antibody, notch5 antibody, wu:fa14b08 antibody, notch 3 antibody, NOTCH3 antibody, Notch3 antibody, notch3 antibody
    Background
    This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Gene ID
    4854
    UniProt
    Q9UM47
    Pathways
    Notch Signaling
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