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  2. Total complement activity - Wikipedia

    en.wikipedia.org/wiki/Total_complement_activity

    The test is based on the capacity of an individual's serum to lyse sheep erythrocytes coated with anti-sheep antibodies (preferably rabbit IgG). The individual's serum is diluted until a minimum concentration of 50% of the sheep's red blood cells are lysed. This is recorded as the CH50.

  3. Complement component 4 - Wikipedia

    en.wikipedia.org/wiki/Complement_component_4

    The cleavage of the C4 results in C4b bearing a thioester functional group [-S-C(O)-]: work in the 1980s on C3, and then on C4, indicated the presence, within the parent C3 and C4 structures, of a unique protein modification, a 15-atom (15-membered) thionolactone ring serving to connect the thiol side chain of the amino acid cysteine (Cys) in a ...

  4. Complement component 3 - Wikipedia

    en.wikipedia.org/wiki/Complement_component_3

    Complement component 3, often simply called C3, is a protein of the immune system that is found primarily in the blood. It plays a central role in the complement system of vertebrate animals and contributes to innate immunity. In humans it is encoded on chromosome 19 by a gene called C3. [5] [6]

  5. Complement 3 deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_3_deficiency

    Complement component 3 (C3) is a protein involved in both the innate and adaptive immune response. C3 is one of over 30 complement proteins circulating in the blood. [3] C3 circulates in an inactive form but can be activated in order to aid the immune system's response to a foreign invader. [4]

  6. Complement deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_deficiency

    C3: In terms of deficiency of C3, it has been found that 17 mutations in the C3 gene cause problems with C3. This rare condition mutates or prevents C3 protein from forming, lowering the immune system's ability to protect. [17] C4: C4 deficiency is highly associated with systemic lupus erythematosus. [3]

  7. Classical complement pathway - Wikipedia

    en.wikipedia.org/wiki/Classical_complement_pathway

    C2b diffuses into the plasma as a protein inflammatory mediator while C2a remains attached with C4b, forming the C3-convertase (C4b2a). The function of the membrane-bound C3-convertase is the cleavage of many many molecules of C3 into C3a and C3b. C3a is a smaller fragment of C3 is a potent inflammatory mediator.

  8. Complement system - Wikipedia

    en.wikipedia.org/wiki/Complement_system

    Scheme of the complement system. The complement system, also known as complement cascade, is a part of the humoral, innate immune system and enhances (complements) the ability of antibodies and phagocytic cells to clear microbes and damaged cells from an organism, promote inflammation, and attack the pathogen's cell membrane. [1]

  9. Nephritic syndrome - Wikipedia

    en.wikipedia.org/wiki/Nephritic_syndrome

    Serum complement (C3 and C4) - Complement factors bind to antibodies to form immune complexes and a decreased serum complement level could indicate that the complement is being consumed at a higher rate due to the formation of immune complexes leading to deposition in the glomerulus of the kidney. [9]