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NOTCH3 antibody (AA 47-156)

This anti-NOTCH3 antibody is a Mouse Monoclonal antibody detecting NOTCH3 in ELISA. Suitable for Human.
Catalog No. ABIN5542534

Quick Overview for NOTCH3 antibody (AA 47-156) (ABIN5542534)

Target

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

Reactivity

  • 55
  • 19
  • 11
  • 1
Human

Host

  • 42
  • 15
  • 3
  • 1
  • 1
Mouse

Clonality

  • 46
  • 17
Monoclonal

Conjugate

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

Application

  • 26
  • 25
  • 22
  • 8
  • 7
  • 4
  • 4
  • 3
  • 2
  • 1
ELISA

Clone

3E2D9
  • Binding Specificity

    • 13
    • 11
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 47-156

    Purpose

    Notch3 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human Notch3 (AA: 47-156) expressed in E. Coli.

    Isotype

    IgG2a
  • Application Notes

    ELISA: 1/10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • 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).

    Molecular Weight

    243.6 kDa

    Gene ID

    4854

    UniProt

    Q9UM47

    Pathways

    Notch Signaling
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