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ALPL antibody (Center)

This Rabbit Polyclonal antibody specifically detects ALPL in . It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN6295240

Quick Overview for ALPL antibody (Center) (ABIN6295240)

Target

See all ALPL Antibodies
ALPL (Alkaline Phosphatase, Liver/bone/kidney (ALPL))

Reactivity

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

Host

  • 92
  • 27
  • 1
  • 1
Rabbit

Clonality

  • 91
  • 30
Polyclonal

Conjugate

  • 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
This ALPL antibody is un-conjugated

Application

Please inquire
  • Binding Specificity

    • 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

    Purpose

    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.
  • Restrictions

    For Research Use only
  • Storage

    4 °C,-20 °C

    Storage Comment

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

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

    Alternative Name

    ALPL

    Background

    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

    Gene ID

    249

    UniProt

    P05186
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