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NOTCH3 anticorps (AA 2291-2321)

Cet anticorps anti-NOTCH3 est un anticorps Souris Monoclonal détectant NOTCH3 dans WB et ELISA. Adapté pour Humain.
N° du produit ABIN3032031

Aperçu rapide pour NOTCH3 anticorps (AA 2291-2321) (ABIN3032031)

Antigène

Voir toutes NOTCH3 Anticorps
NOTCH3 (Notch 3 (NOTCH3))

Reactivité

  • 58
  • 20
  • 11
  • 1
Humain

Hôte

  • 42
  • 18
  • 4
  • 1
  • 1
Souris

Clonalité

  • 46
  • 21
Monoclonal

Conjugué

  • 34
  • 5
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
Cet anticorp NOTCH3 est non-conjugé

Application

  • 26
  • 24
  • 22
  • 11
  • 7
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA

Clone

487CT6-9-2
  • Épitope

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

    Purification

    Purified

    Immunogène

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

    Isotype

    IgG1
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Aliquot the NOTCH3 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Antigène

    NOTCH3 (Notch 3 (NOTCH3))

    Autre désignation

    NOTCH3

    Sujet

    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

    Signalisation Notch
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