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ALPL Antikörper (Center)

Dieses Kaninchen Polyklonal-Antikörper erkennt spezifisch ALPL in . Er zeigt eine Reaktivität gegenüber Human und Maus.
Produktnummer ABIN6295240

Kurzübersicht für ALPL Antikörper (Center) (ABIN6295240)

Target

Alle ALPL Antikörper anzeigen
ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Reaktivität

  • 95
  • 56
  • 21
  • 7
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Maus

Wirt

  • 92
  • 27
  • 1
  • 1
Kaninchen

Klonalität

  • 91
  • 30
Polyklonal

Konjugat

  • 76
  • 10
  • 7
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ALPL Antikörper ist unkonjugiert

Applikation

Bitte anfragen
  • Bindungsspezifität

    • 16
    • 13
    • 10
    • 9
    • 5
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 217-246, Center

    Verwendungszweck

    Rabbit Anti-ALPL (Center) Antibody

    Immunogen

    This ALPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 217-246 amino acids from the Central region of human ALPL.
  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    2-8°C (short-term), -20°C (long-term)
  • Target

    ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

    Andere Bezeichnung

    ALPL

    Hintergrund

    Target Description: There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The genes for the first three are located together on chromosome 2 while the tissue non-specific form is located on chromosome 1. This protein is a membrane bound glycosylated enzyme that is not expressed in any particular tissue and is, therefore, referred to as the tissue-nonspecific form of the enzyme. The exact physiological function of the alkaline phosphatases is not known. A proposed function of this form of the enzyme is matrix mineralization, however, mice that lack a functional form of this enzyme show normal skeletal development. This enzyme has been linked directly to a disorder known as hypophosphatasia, a disorder that is characterized by hypercalcemia and includes skeletal defects. The character of this disorder can vary, however, depending on the specific mutation since this determines age of onset and severity of symptoms.

    Gene Symbol: ALPL

    Gen-ID

    249

    UniProt

    P05186
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