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Glypican 3 Antikörper

Dieses Anti-Glypican 3-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Glypican 3 in IHC. Geeignet für Human, Ratte und Maus.
Produktnummer ABIN7008556

Kurzübersicht für Glypican 3 Antikörper (ABIN7008556)

Target

Alle Glypican 3 (GPC3) Antikörper anzeigen
Glypican 3 (GPC3)

Reaktivität

  • 184
  • 63
  • 49
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Ratte, Maus

Wirt

  • 110
  • 73
  • 5
  • 2
  • 1
  • 1
Kaninchen

Klonalität

  • 97
  • 87
  • 5
Polyklonal

Konjugat

  • 87
  • 15
  • 7
  • 7
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Glypican 3 Antikörper ist unkonjugiert

Applikation

  • 97
  • 87
  • 85
  • 68
  • 58
  • 30
  • 26
  • 18
  • 15
  • 15
  • 6
  • 2
  • 2
  • 1
  • 1
Immunohistochemistry (IHC)
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Affinity purification

    Immunogen

    Recombinant fusion protein of human GPC3 (NP_004475.1).

    Isotyp

    IgG
  • Applikationshinweise

    IHC 1:50-1:200

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Glypican 3 (GPC3)

    Andere Bezeichnung

    GPC3

    Hintergrund

    Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains. Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage. These proteins may play a role in the control of cell division and growth regulation. The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types. Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome. Alternative splicing results in multiple transcript variants.

    Gen-ID

    2719

    UniProt

    P51654

    Pathways

    Glycosaminoglycan Metabolic Process
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