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NOTCH3 antibody (AA 2291-2321)

This anti-NOTCH3 antibody is a Mouse Monoclonal antibody detecting NOTCH3 in WB and ELISA. Suitable for Human.
Catalog No. ABIN3032031

Quick Overview for NOTCH3 antibody (AA 2291-2321) (ABIN3032031)

Target

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

Reactivity

  • 56
  • 19
  • 11
  • 1
Human

Host

  • 43
  • 15
  • 3
  • 1
  • 1
Mouse

Clonality

  • 47
  • 17
Monoclonal

Conjugate

  • 33
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This NOTCH3 antibody is un-conjugated

Application

  • 26
  • 25
  • 23
  • 8
  • 7
  • 5
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA

Clone

487CT6-9-2
  • Binding Specificity

    • 13
    • 10
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 2291-2321

    Purification

    Purified

    Immunogen

    A portion of amino acids 2291-2321 from the human protein was used as the immunogen for this NOTCH3 antibody.

    Isotype

    IgG1
  • Application Notes

    Titration of the NOTCH3 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:100-1:250

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Storage Comment

    Aliquot the NOTCH3 antibody and store frozen at -20°C or colder. Avoid repeated 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). [provided by RefSeq].

    UniProt

    Q9UM47

    Pathways

    Notch Signaling
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