Complement iC3b, Complement component 3b inactive

Human

CSI19504 pdf (datasheet)

250 μg

$525.00 BUY

iC3b (inactivated C3b) is derived from C3b. Conversion of C3b to iC3b destroys almost all of the functional binding sites present on C3b. C3b itself is produced by all three pathways of complement when native C3 is cleaved releasing C3a. iC3b is prepared by cleavage of C3b by factor I in the presence of factor H. Cleavage by factors H and I occurs rapidly when the C3b is free in solution and is slower when it is attached to a surface. Other cofactors for factor I also permit cleavage if C3b to iC3b and these include the two membrane proteins CR1 (CD35) and MCP (CD46). Factor I can cleave C3b in two places in the alpha chain and if both sites are cleaved a small fragment (C3f, 2,000 Da) is released. If the C3b precursor was attached to a surface, the iC3b remains on that surface. This iC3b is made from fluid phase C3b and is not capable of attaching to a surface. Surface-bound iC3b and its breakdown product C3d are recognized by numerous receptors on lymphoid and phagocytic cells which use these ligands to stimulate phagocytosis and antigen presentation to cells of the adaptive immune system. Receptors for iC3b are CR2 (CD21) found on B-cells and CR3 (CD11b/CD18) found on phagocytes. One of the results of iC3b-receptor interaction is an expansion of target-specific B-cell and T-cell populations.

1.0 mg/ml, lot specific

C3

Complement C3

P01024

CSI19504

Human Serum

176 kDa three chains

Sterile-filtered PBS, pH 7.2

>95% by SDS-PAGE, trace IgG, IgA, IgM, albumin, C5, Factor B, Factor H, Factor I by immunochemistry.

Store as supplied at -80°C for up to 1 year.