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AssayPro—Human C-Reactive Prot

ein ELISA Kit(人C反应蛋白酶联免疫试剂盒)
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  • ¥3920
  • AssayPro
  • 0.25 ng/ml
  • 美国
  • EC1001-1
  • 2025年12月14日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 供应商

      AssayPro

    • 检测范围

      0.25 ng/ml

    • 检测方法

      ELISA

    • 应用

      血清、血浆、细胞培养上清液、尿液、唾液、牛奶

    • 样本

      50 μl

    • 规格

      96 wells

    AssayMax Human C-Reactive Protein ELISA Kit
    人C反应蛋白酶联免疫试剂盒

    Introduction
    C-Reactive Protein (CRP) is a liver protein composed of five identical non-glycosylated subunits, with a total molecular weight of 105 kDa. CRP has a variety of powerful effects related to immunology, inflammation, and coagulation. As a marker of low-level inflammation, CRP appears to predict future cardiovascular disease events among apparently healthy individuals. High plasma concentration of CRP was associated with increased risk of stroke, myocardial infarction, and peripheral vascular disease (1-3). CRP has also been associated with increased risks of fatal coronary events among high-risk male smokers and incident coronary disease among the elderly (4, 5). Studies have established the prognostic usefulness of CRP in the setting of angina (6). Originally used as a marker of acute inflammation, CRP has become a leading candidate as the measure of choice for estimating the inflammatory component of cardiovascular disease risk.

    Principle of the Assay
    The AssayMax Human C-Reactive Protein ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of human CRP in plasma, serum, saliva, milk, urine, and cell culture samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures CRP in less than 4 hours. A murine antibody specific for CRP has been pre-coated onto a 96-well microplate with removable strips. CRP in standards and samples is sandwiched by the immobilized antibody and biotinylated polyclonal antibody specific for CRP, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.

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