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NOTCH3 antibody

This Rabbit Polyclonal antibody specifically detects NOTCH3 in WB and IF. It exhibits reactivity toward Humanand has been mentioned in 1 publication.
Catalog No. ABIN3023484

Quick Overview for NOTCH3 antibody (ABIN3023484)

Target

See all NOTCH3 Antibodies
NOTCH3 (Notch 3 (NOTCH3))

Reactivity

  • 55
  • 19
  • 11
  • 1
Human

Host

  • 41
  • 16
  • 3
  • 1
  • 1
Rabbit

Clonality

  • 45
  • 18
Polyclonal

Conjugate

  • 32
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This NOTCH3 antibody is un-conjugated

Application

  • 27
  • 24
  • 22
  • 8
  • 6
  • 4
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    A synthetic peptide of human NOTCH3

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 1:1000,IF,1:50 - 1:200

    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.
  • Zhou, Jiang, Dong, Yan, You, Su, Gong: "The proteins interacting with C-terminal of μ receptor are identified by bacterial two-hybrid system from brain cDNA library in morphine-dependent rats." in: Life sciences, Vol. 143, pp. 156-67, (2016) (PubMed).

  • Target

    NOTCH3 (Notch 3 (NOTCH3))

    Alternative Name

    NOTCH3

    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).,NOTCH3,CADASIL,CADASIL1,CASIL,IMF2,LMNS,notch 3,Epigenetics & Nuclear Signaling,Transcription Factors,Signal Transduction,Cell Biology & Developmental Biology,Cell Cycle,Cell differentiation,Notch Signaling Pathway,ESC Pluripotency and Differentiation,Neuroscience,Stem Cells,Hematopoietic Progenitors,Neural Stem Cells,Cardiovascular,Heart,Cardiogenesis,NOTCH3

    Molecular Weight

    243 kDa

    Gene ID

    4854

    UniProt

    Q9UM47

    Pathways

    Notch Signaling
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