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CDw17 anticorps

L’anticorps Souris Monoclonal anti-not_set a été validé pour FACS et IF. Il convient pour détecter not_set dans des échantillons de Humain.
N° du produit ABIN6296201
714,43 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 10 à 13 jours ouvrables

Aperçu rapide pour CDw17 anticorps (ABIN6296201)

Antigène

CDw17

Reactivité

Humain

Hôte

  • 4
Souris

Clonalité

  • 4
Monoclonal

Conjugué

  • 4
Inconjugué

Application

  • 4
  • 4
  • 1
  • 1
Flow Cytometry (FACS), Immunofluorescence (IF)
  • Fonction

    Mouse anti-Human CDw17 Antibody [Sodium Azide Free]

    Specificité

    Cell surface

    Purification

    Beta-2 Microglobulin associated proteins from a detergent lysate of human PBLs were used as the immunogen for the CDw17 antibody.

    Immunogène

    Beta-2 Microglobulin associated proteins from a detergent lysate of human PBLs were used as the immunogen for the CDw17 antibody.
  • Indications d'application

    Flow Cytometry: 0.5-1 μg/million cells in 0.1ml
    Immunofluorescence: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    In 1X PBS, BSA free, sodium azide free

    Agent conservateur

    Azide free

    Stock

    4 °C,-20 °C

    Stockage commentaire

    2-8°C. The azide-free format should be aliquoted and stored at -20°C or colder.
  • Antigène

    CDw17

    Sujet

    Target Description: CD17 is an intermediate glycosphingolipid from the metabolism of higher gangliosides that localizes to sphingolipid-sterol rafts. CD17 is detectable in monocytes, granulocytes, basophils, platelets, a subset of peripheral B cells (CD19+) and tonsil dendritic cells. It is rapidly down regulated on activated granulocytes and is upregulated on IL-2 activated T lymphocytes. CD17 binds to bacteria and may function in phagocytosis. VEGF-treated endothelial cells can produce CD17, which can then mediate signaling toward PECAM-1 expression and angiogenesis. TNFa-induced astrogliosis (astrocyte proliferation and glial fibrillary acidic protein (GFAP) upregulation) in response to neuro-inflammation (i.e. spinal cord injury) causes an increase in intracellular levels of CD17. Aberrant levels of glycosphingolipids are a feature of cancer cells and may influence integrin clustering and internalization.

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