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NOTCH3 Antikörper (AA 2291-2321)

Dieses Anti-NOTCH3-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von NOTCH3 in WB und ELISA. Geeignet für Human.
Produktnummer ABIN3032031

Kurzübersicht für NOTCH3 Antikörper (AA 2291-2321) (ABIN3032031)

Target

Alle NOTCH3 Antikörper anzeigen
NOTCH3 (Notch 3 (NOTCH3))

Reaktivität

  • 59
  • 20
  • 11
  • 1
Human

Wirt

  • 43
  • 18
  • 4
  • 1
  • 1
Maus

Klonalität

  • 47
  • 21
Monoklonal

Konjugat

  • 35
  • 5
  • 4
  • 4
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
Dieser NOTCH3 Antikörper ist unkonjugiert

Applikation

  • 26
  • 25
  • 23
  • 11
  • 7
  • 5
  • 5
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA

Klon

487CT6-9-2
  • Bindungsspezifität

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

    Aufreinigung

    Purified

    Immunogen

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

    Isotyp

    IgG1
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % sodium azide

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    NOTCH3 (Notch 3 (NOTCH3))

    Andere Bezeichnung

    NOTCH3

    Hintergrund

    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 Signalweg
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