补充技术/小鼠C3b/1.0 mg/ml/M114

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¥6300.00
货号:M114
浏览量:127
品牌:Complement
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Product Description

Mouse C3b is derived from native purified mouse C3 (CompTech #M113) upon cleavage and release of C3a with the alternative pathway C3 convertase. C3 is central to the activation of all three pathways of complement activation (Law, S.K.A. and Reid, K.B.M. (1995)). Initiation of each pathway generates proteolytic enzyme complexes (C3 convertases) which are bound to the target surface. These enzymes cleave a peptide bond in C3 releasing the anaphylatoxin C3a and activating C3b. For a brief time (~60 µs) this nascent C3b is capable of reacting with and covalently coupling to hydroxyl groups on the target surface. Carbohydrates are the favored target, but protein hydroxyls and amino groups also react. This process of tagging the target surface with C3b is called opsonization. The reactive site in nascent C3b is a thioester (Tack B.J., et al. (1980); Pangburn M.K. and MüllerEberhard H.J. (1980)) and C3b is linked to the target through a covalent ester bond (an amide bond is formed if C3b is attached to amino groups). Most of the C3 activated during complement activation never attaches to the surface because its thioester reacts with water forming fluid phase C3b which is rapidly inactivated by factors H and I forming iC3b. Surface-bound C3b is necessary in all three pathways for efficient activation of C5 and formation of C5b-9 complexes that lyse the target cell membrane. Surface-bound C3b and its breakdown products iC3b and C3d are recognized by numerous receptors on lymphoid and phagocytic cells which use the C3b ligand to stimulate antigen presentation to cells of the adaptive immune system. The end result is an expansion of target-specific B-cell and T-cell populations.

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Complement Technology的C1是级联反应中的第一个补体成分,称为补体经典途径。C1与抗原结合的抗体(免疫复合物)结合并被其激活,从而产生引发级联反应的蛋白酶。C1实际上是钙依赖性复合物中结合在一起的三种不同蛋白质(C1q,C1r和C1s)的非共价复合物。C1q通过其六个臂中的两个或多个与IgG或IgM的Fc结构域结合。多臂与免疫复合物的结合被认为会引入压力,从而导致复合物中的两个C1r蛋白(蛋白酶酶原)自身激活,从而产生两种活性的C1r丝氨酸蛋白酶(Morikis,D.和Lambris,JD(2005))。 。这些激活的C1r亚基裂解并激活复合物中的两个C1s蛋白酶酶原。活化的C1裂解补体成分C4,释放出C4a,并启动C4b与活化表面的共价连接。活化的C1也切割C2,并且C2的较大片段结合至表面附着的C4b,形成C4b,C2a,其为经典途径的C3 / C5转化酶。