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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:
0.1 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
补体C1酶联免疫试剂盒
Introduction
Complement component C1 (C1) is a calcium-dependent serine protease complex with an approximate mass of 790 kDa and acts as the first component of the classical complement pathway. C1 is formed from the association of a recognition protein C1q and two catalytic subunits C1r and C1s respectively (1 - 2). The globular heads of the C1q bind to the Fc-fragment of IgM or IgG on the surface of a pathogen, resulting in the activation of C1r. The activated C1r is able to activate C1s which in turn activates C2 and C4, leading to the production of the C4b-C2a form of C3-convertase (3 - 4). C1 deficiency is generally associated with severe immune complex disease of systemic lupus erythematosus and glomerulonephritis (5 - 6).
Principle of the Assay
The AssayMax Human Complement C1 ELISA kit is designed for detection of C1 in human plasma, serum, saliva, urine, milk, and cell culture samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures C1 in less than 4 hours. A polyclonal antibody specific for C1 has been pre-coated onto a microplate. C1 in standards and samples is sandwiched by the immobilized antibody and a biotinylated polyclonal antibody specific for C1, 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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文献和实验亚单位(链)及分子量(kDa):1条 激活产物:C1r� 生物学活性:丝氨酸蛋白酶,裂解C1s 补体成分:C1s 血清浓度(μg/ml):50 分子量(kDa):85 亚单位(链)及分子量(kDa):1条 激活产物:C1s� 生物学活性:丝氨酸蛋白酶,裂解C4、C2 ELISA KIT
The classical complement pathway (CCP) activation is a multimolecular complex, composed of three subcomponents namely C1q, C1r, and C1s. C1q is the recognition subunit of this complex and its binding to the specific targets leads
C1r and C1s are the proteases responsible for the activation and proteolytic activity of the C1 complex of the classical complement pathway, respectively. They are assembled into a Ca2+ -dependent C1s–C1r–C1r–C1s tetramer which in turn
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