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CDw17 antibody

The Mouse Monoclonal anti-CDw17 antibody has been validated for FACS and IF. It is suitable to detect CDw17 in samples from Human.
Catalog No. ABIN6296201
$739.45
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 6 to 8 Business Days

Quick Overview for CDw17 antibody (ABIN6296201)

Target

CDw17

Reactivity

Human

Host

  • 4
Mouse

Clonality

  • 4
Monoclonal

Conjugate

  • 4
Un-conjugated

Application

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

    Mouse anti-Human CDw17 Antibody [Sodium Azide Free]

    Specificity

    Cell surface

    Purification

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

    Immunogen

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

    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

    Preservative

    Azide free

    Storage

    4 °C,-20 °C

    Storage Comment

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

    CDw17

    Background

    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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