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產(chǎn)品名稱: MicroVue C5a EIA
產(chǎn)品型號(hào): A021
產(chǎn)品展商: Quidel Corporation
產(chǎn)品文檔: 無(wú)相關(guān)文檔
簡(jiǎn)單介紹
The MicroVue C5a Enzyme Immunoassay measures the amount of C5a-des-Arg present in human serum, plasma and other biological or experimental samples.
MicroVue C5a EIA
的詳細(xì)介紹
For Research Use Only in the United States. Not for use in diagnostic procedures.
The MicroVue C5a Enzyme Immunoassay measures the amount of C5a-des-Arg present in human serum, plasma and other biological or experimental samples.
Complement protein C5 is unique to the terminal complement pathway and under normal conditions is cleaved by a C5 convertase to C5a and C5b as a result of activation of the classical, alternative or lectin complement pathway.
Research has shown that elevated levels of C5a have been associated with pathogenesis of a variety of disease states including myocardial infarction, stroke and kidney injury. The role of C5a in the pathogenesis of malaria and other infectious diseases as well as sepsis is likewise well documented.
The MicroVue C5a Enzyme Immunoassay measures the concentration of C5a in human plasma, serum and other experimental samples. It uses a proprietary monoclonal antibody to a neo-epitope on C5a to capture C5a in solid phase. The trapped C5a is then detected by HRP-labeled antibodies to C5a antigens. This test provides a quantitative measurement of C5a levels and is designed for investigations into the role and status of terminal complement pathway activation in numerous clinical and research settings.
References:
Arbesu I, Bucsaiova M, Fischer MB, Mannhalter C. Platelet-borne complement proteins and their role in platelet–bacteria interactions. J Thromb Haemost 2016; 14: 2241–52.
Wang G, Chen F, Banda NK, Holers VM, Wu L, Moghimi SM and Simberg D (2016) Activation of Human Complement System by Dextran-Coated Iron Oxide Nanoparticles Is Not Affected by Dextran/Fe Ratio, Hydroxyl Modifications, and Crosslinking. Front. Immunol. 7:418. doi: 10.3389/fimmu.2016.00418
