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CDw17 Antikörper

Dieser Anti-CDw17-Antikörper ist ein Maus-Monoklonal-Antikörper zum Nachweis von CDw17 in FACS und IF. Geeignet für Human.
Produktnummer ABIN3024298
642,40 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 8 Werktagen

Kurzübersicht für CDw17 Antikörper (ABIN3024298)

Target

CDw17

Reaktivität

Human

Wirt

  • 4
Maus

Klonalität

  • 4
Monoklonal

Konjugat

  • 4
Unkonjugiert

Applikation

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

Klon

HO18-3G-6-F5
  • Aufreinigung

    PEG precipitation

    Immunogen

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

    Isotyp

    IgM
  • Applikationshinweise

    Optimal dilution of the CDw17 antibody should be determined by the researcher.\. Flow Cytometry: 0.5-1 μg/million cells in 0.1ml,Immunofluorescence: 0.5-1 μg/mL

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1 mg/mL

    Buffer

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    Konservierungsmittel

    Azide free

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    Store the CDw17 antibody at 2-8°C (with azide) or aliquot and store at -20°C or colder (without azide).
  • Target

    CDw17

    Hintergrund

    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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