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Human Nicotinamide Adenine Din

ucleotide Phosphate Oxidase 2 (NOX2) ELISA Kit试剂盒,orb1088211,biorbyt
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  • ¥3900
  • biorbyt已认证
  • 0.16-10 ng/mL
  • 0.058 ng/mL
  • orb1088211
  • 英国
  • 2026年01月21日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      999

    • 供应商

      biorbyt

    • 检测范围

      0.16-10 ng/mL

    • 检测方法

      Sandwich

    • 适应物种

      Human

    • 样本

      Tissue homogenates, cell lysates and other biological fluids

    • 灵敏度

      0.058 ng/mL

    • 规格

      48 T

    产品描述:The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Nicotinamide Adenine Dinucleotide Phosphate Oxidase 2(NOX2). Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Nicotinamide Adenine Dinucleotide Phosphate Oxidase 2(NOX2). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Nicotinamide Adenine Dinucleotide Phosphate Oxidase 2(NOX2), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Nicotinamide Adenine Dinucleotide Phosphate Oxidase 2(NOX2) in the samples is then determined by comparing the OD of the samples to the standard curve.

    产品别名:NADPH Oxidase 2, NOX2

    应用笔记:standard: 10 ng/mL. Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human NOX2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NOX2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human NOX2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human NOX2 in the samples is then determined by comparing the OD of the samples to the standard curve

    实验时长:3.5h

    Note:For research use only.

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    图标文献和实验
    相关实验
    • A Microtiter-Plate Assay of Human NOS Isoforms

      Nitric oxide synthase (NOS) catalyzes the conversion of L -arginine, molecular oxygen, and nicotinamide adenine dinucleotide phosphate (NADPH) to NO, citrulline, and NADP+ (reviewed in ref. 1 ). The neuronal (n) and endothelial (e) NOS

    • Cloning and Expression of Human eNOS and nNOS Using the Baculovirus-Insect Cell System

      as a co-product and requires the presence of heme, tetrahydrobiopterin (BH4 ), nicotinamide adenine dinucleotide phosphate (NADPH), calmodulin (CaM), flavin mononucleotide (FMN), and flavine adenine nucleotide (FAD) (2 ). The NO generated by the family

    • Reactive Oxygen Release

      Monocytes, macrophages, neutrophils, and eosinophils are able to generate and release reactive oxygen species. The reactive oxygen species are generated by reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase which is activated

    图标技术资料

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