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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:
1 ng/ml
- 检测方法:
ELISA
- 应用:
细胞培养上清液、尿液、唾液、牛奶
- 样本:
50 μl
- 规格:
96 wells
人铜蓝蛋白CP酶联免疫试剂盒
Introduction
Ceruloplasmin is an abundant α2-serum glycoprotein that contains 95% of the copper found in the plasma of vertebrate species (1). Ceruloplasmin is a copper-binding protein that normally removes iron from cells by its ferroxidase activity. Ceruloplasmin concentration on average is 14.6 (±4.0) mg/dl (2). Low levels of ceruloplasmin lead to the abnormal deposition of iron in cells, including those of the pancreas, liver, retina and the basal ganglia region of the brain. Some diseases associated with ceruloplasmin are Wilson's disease (3), Hemochromatosis (4), Menkes disease, (5) and Aceroluplasminemia (1).
Principle of the Assay
The AssayMax Human Ceruloplasmin ELISA kit is designed for detection of ceruloplasmin in human urine, saliva, milk, and cell culture supernatant. This assay employs a quantitative sandwich enzyme immunoassay technique that measures ceruloplasmin in less than 4 hours. A polyclonal antibody specific for ceruloplasmin has been pre-coated onto a microplate. Ceruloplasmin in standards and samples is sandwiched by the immobilized antibody and a biotinylated polyclonal antibody specific for ceruloplasmin, 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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文献和实验consists of a cooperation between monocytes and cytophilic antibodies able to bind to the Fc receptors present on the monocyte surface. Thus human IgG1 and IgG3 are the main isotypes effective in ADCI, whereas IgG2, IgG4, and IgM are ineffective
Human Xanthine Oxidoreductase Determination by a Competitive ELISA
Xanthine oxidoreductase (XO) catalyses the oxidation of hypoxanthine to xanthine and of the latter to uric acid. The enzyme is present in traces in most of human tissues, including plasma, being more abundant in milk, liver, and intestine (1).
Quantification of Human IgG and Related Fc Fusion Proteins by a Human IgG/Fc Capture ELISA
of recombinant human IgGs after production and purification for further assays. Here, we describe a human IgG/Fc capture enzyme linked immunosorbent assay (ELISA) which is simple, robust, inexpensive and specific for all types of human IgGs and related Fc fusion
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