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FGF13 Antikörper

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch FGF13 in IHC und ELISA. Er zeigt eine Reaktivität gegenüber Human, Ratte und Maus.
Produktnummer ABIN7244969

Kurzübersicht für FGF13 Antikörper (ABIN7244969)

Target

Alle FGF13 Antikörper anzeigen
FGF13 (Fibroblast Growth Factor 13 (FGF13))

Reaktivität

  • 91
  • 17
  • 15
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Ratte, Maus

Wirt

  • 67
  • 40
  • 1
Kaninchen

Klonalität

  • 71
  • 37
Polyklonal

Konjugat

  • 57
  • 9
  • 9
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser FGF13 Antikörper ist unkonjugiert

Applikation

  • 78
  • 61
  • 44
  • 28
  • 22
  • 17
  • 13
  • 13
  • 5
  • 4
  • 3
  • 1
  • 1
Immunohistochemistry (IHC), ELISA
  • Produktmerkmale

    Polyclonal Antibody

    Aufreinigung

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human FGF13

    Isotyp

    IgG
  • Applikationshinweise

    IHC 1:40-1:200, ELISA 1:5000-1:10000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    1.26 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    FGF13 (Fibroblast Growth Factor 13 (FGF13))

    Andere Bezeichnung

    FGF13

    Hintergrund

    The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.

    UniProt

    Q92913

    Pathways

    Regulation of Cell Size
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