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Rat/Mouse Apolipoprotein CIII

ELISA Kit(大鼠/小鼠载脂蛋白Apo-CIII酶联免疫试剂盒)
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  • ¥4480
  • AssayMax
  • 0.5 μg/ml
  • 美国
  • ERA9133-1
  • 2025年12月12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

      0.5 μg/ml

    • 检测方法

      ELISA

    • 应用

      血清、血浆、细胞培养上清液、细胞裂解液

    • 样本

      25 μl

    • 规格

      96 wells

    AssayMax Rat/Mouse Apolipoprotein CIII(Apo CIII) ELISA Kit
    大鼠/小鼠载脂蛋白Apo-CIII酶联免疫试剂盒

    Introduction
    Apolipoprotein C-III (ApoC-III) is a surface component of chylomicrons, very low density lipoproteins, and high density lipoproteins. It consists of 79 amino acids with a molecular mass of 8.8 kDa (1). ApoC-III is synthesized mainly in the liver and to a lesser degree in the intestine. It plays a key role in triglyceride-rich lipoprotein metabolism. It is an inhibitor of lipoprotein lipase and hepatic lipase and interferes with binding of lipoproteins to cell surface heparan sulfate proteoglycans and receptors (2, 3). Overexpression of the human apoC-III gene causes hypertriglyceridemia in transgenic mice (4, 5). Deficiency of apoC-III prevents hyperlipidemia induced by apoE overexpression (6). As its deficiency results in diet-induced obesity and aggravated insulin resistance in mice, ApoC-III is a potential target for treatment of obesity and insulin resistance (7).

    Principle of the Assay
    The AssayMax Rat/Mouse Apolipoprotein C-III ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for detection of rat/mouse apoC-III in plasma, serum, and cell culture samples. This assay employs a quantitative competitive enzyme immunoassay technique that measures rat/mouse apoC-III in less than 5 hours. A capture antibody has been coated onto a 96-well microplate with removable strips. A specific antibody against rat apoC-III binds to the captured antibody. ApoC-III in standards and samples is competed with a biotinylated apoC-III sandwiched by the immobilized antibody and 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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      isolation kit, Qiagen), pooled mRNA for each treatment group. As well as GAPDH, factor VII, glucose-6-phosphatase and VEGF mRNAs were also used for normalization. ELISA was used to quantify the reduction of apoB-100 protein levels in mouse plasma

    • secondary antibody review -- data from 99 publications

      epithelial Caco2/bbe cells Bio-Rad 10       rhodamine immunocytochemistry 1:100 detect phospho-CREB in human colonic epithelial Caco2/bbe cells Bio-Rad 11 goat IgG   FITC immunohistochemistry 1:40 detect ameloblastin in mouse postnatal mandibular molars

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