anti-Complement C1q, mAb (9A7)

CHF 315.00
In stock
YIF-LF-MA0258100 µlCHF 315.00
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Product Details
Synonyms C1QA; Complement C1q Subcomponent Subunit A
Product Type Monoclonal Antibody
Clone 9A7
Isotype Mouse IgG2b κ
Immunogen/Antigen Protein purified from human plasma.

Western Blot (1:1,000)

Crossreactivity Human
Purity Detail Ammonium sulfate precipitation.
Formulation Liquid. HEPES with 0.15M NaCl, 0.01% BSA, 0.03% sodium azide, and 50% glycerol.
Isotype Negative Control

Mouse IgG2b Isotype Control

Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

Declaration Manufactured by AbFrontier
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Use/Stability Stable for at least 1 year after receipt when stored at -20°C.
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Product Specification Sheet
Datasheet Download PDF

The complement system is a part of the larger immune system and three biochemical pathways are present: the classical complement pathway, the alternative pathway, and the mannose-binding lectin pathway. The biological functions of complement are opsonization and phagocytosis, stimulation of inflammatory reactions and lysis of bacteria. C1 complex (C1q, C1r and C1s) is the first component of the classical pathway of complement activation which occurs when C1q binds to IgM or IgG complexed with antigens, or when C1q binds directly to the surface of the pathogen. Binding of C1 to immunoglobulins in the form of immune complexes leads to activation of proteases C1r and C1s, and the cleavage of C2 and C4 producing C2a and C4b. C4b and C2a bind to form C3-convertase. C1q is a hexamer composed of globular heads attached to collagen-like triple-helix tails. The globular heads of C1q specifically bind to the CH2 domain of IgG molecules or the CH3 domain of IgM. In mammals, hepatocyte is the major source of most C proteins with the exception of C1q, factor D and C7. Interestingly, C1q mRNA is essentially expressed in spleen, thymus and heart. C1q knockout mice show a profound impairment in the clearance of apoptotic cells which then accumulate in the kidney leading to glomerulonephritis with immune deposits. Individuals with deficiency of C1q have the highest prevalence of systemic lupus erythematosus. C1q associates with the proenzymes C1r and C1s to yield C1, the first component of the serum complement system. The collagen-like regions of C1q interact with the Ca2+-dependent C1r2C1s2 proenzyme complex, and efficient activation of C1 takes place on interaction of the globular heads of C1q with the Fc regions of IgG or IgM antibody present in immune complexes.

Product References

1) Potlukova E and Kralikova P, (2008) Scand J Immunol. 67(5):423-430. (General)
2) Gasque P, (2004) Mol Immunol. 41(11) :1089-1098. (General)
3) Botto M and Walport MJ, (2002) Immunobiology. 205(4-5):395-406. (General)

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