> 补体系统 补体系统
Sino biological offers a comprehensive set of tools for research on complement system.
These high-quality reagents include:
| Product Categories / Species | Human | Mouse |
| Recombinant Proteins | 11 | 1 |
| Antibodies | 6 | - |
| ORF cDNA Clones | 12 | 4 |
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补体系统背景综述
The complement system is an enzyme cascade that is a collection of blood and cell surface proteins to help the abilities of antibodies to clear pathogens from an organism. The complement system that comprises 30 different proteins, including serum proteins, serosal proteins, and cell membrane receptors is an important part of the innate immune system. Some complement proteins bind to immunoglobulins or to membrane components of cells. Others are proenzymes that, when activated, cleave one or more other complement proteins and initiate an amplifying cascade of further cleavages. The end-result of this cascade is massive amplification of the response and activation of the cell-killing membrane attack complex. The complement system has four major function, including lysis of infectious organisms, activation of inflammation, opsonization and immune clearance.
There are three different complement pathways, the classical complement pathway, the alternative complement pathway, and the mannose-binding lectin pathway. The classic complement pathway is triggered when antibody-antigen complex interact with C1-complex, which consists of C1q, two molecules of C1r, and two molecules of C1s. The C1-complex cleaves C2 and C4, which then form C3 convertase (C4b2a). C3 is then cleaved by the C3 convertase, and forms C5 convertase in association with C4b and C2a. The generation of C5 convertase is the end of the classical pathway. The lectin pathway is very similar to the classical pathway. It is stimulated when the mannose-binding lectin (MBL) binds to mannose residues on the pathogen surface. The MBL-associated serine proteases, MASP-1, and MASP-2, are activated and cleave C4 and C2, which then form the C3 convertase as in the classical pathway. The alternative complement pathway begins with the activation of C3 and requires factor B and factor D. All three pathways merge at C3, which is then converted into C3a and C3b. The further formed C5 convertase from C3b cleaves C5 into C5a and C5b. C5b with C6, C7, C8, and C9 complex to form the membrane attack complex (MAC), which is inserted into the cell membrane, forms a hole in the membrane, and initiates cells lysis.
补体系统参考文献
- Rus H, et al. (2006) The complement system in central nervous system diseases. Autoimmunity. 39(5):395-402.
- Endo Y, et al. (2006) Lectin complement system and pattern recognition. Immunobiology. 211(4):283-93.
- Basta M. (2008) Ambivalent effect of immunoglobulins on the complement system: activation versus inhibition. Mol Immunol. 45(16):4073-9.
- Morrison TE, et al. (2008) The host complement system and arbovirus pathogenesis. Curr Drug Targets. 9(2):165-72.


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