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Anti-ALPL antibody

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  • 询价
  • 晶抗生物
  • JK220062
  • 上海
  • 2025年09月09日
  • 科研试验
  • Rabbit
  • Human,Mouse,Rat,Chicken,Dog,Cow,Rabbit,Sheep
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商

      上海晶抗生物工程有限公司

    • 库存

      大量

    • 克隆性

      多克隆

    • 保质期

      1年

    • 抗体英文名

      Anti-ALPL antibody

    • 宿主

      Rabbit

    • 适应物种

      Human,Mouse,Rat,Chicken,Dog,Cow,Rabbit,Sheep

    • 应用范围

      科研试验

    • 保存条件

      -20°C

    • 规格

      25 μl/100 μl/200 μl

    Anti-ALPL antibody


    Cat. No.     JK220062      
    Package    25 μl/100 μl/200 μl
    Storage    -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol

    Product overview
    Description                   Anti-ALPL rabbit polyclonal antibody
    Applications        ELISA, IHC 
    Immunogen               Fusion protein of human ALPL
    Reactivity                 Human, Mouse, Rat
    Content                     1.4 mg/ml
    Host species               Rabbit
    Ig class                  Immunogen-specific rabbit IgG
    Purification                 Antigen affinity purification

    Target information
    Symbol                 ALPL
    Full name                 Alkaline phosphatase
    Synonyms    HOPS,TNSALP
    Swissprot    P05186

    Target Background
    There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The first three are located together on chromosome 2, while the tissue non-specific form is located on chromosome 1. The product of this gene 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 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. Alternatively spliced transcript variants have been described.


     

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