Lambris J D, Ross G D
J Immunol. 1982 Jan;128(1):186-9.
A sensitive and specific fluorescence assay for membrane complement (C) receptors (CR1 and CR2) was developed with purified C3b and C3d fragments coupled to fluorescent microspheres (0.9 mu diameter). C3-microspheres (C3-ms) bound to cells with low numbers of receptors that were undetectable by other assay techniques. Inhibition studies with anti-CR1 and anti-CR2 demonstrated that C3b-ms and C3d-ms bound exclusively to CR1 and CR2, respectively. Preparation of the C3-ms required only small amounts of partially purified C3 and no immunoglobulin or other C components. Once formed, the C3-ms were stable for up to 4 mo at 4 degrees C.
利用与荧光微球(直径0.9微米)偶联的纯化C3b和C3d片段,开发了一种用于检测膜补体(C)受体(CR1和CR2)的灵敏且特异的荧光测定法。C3微球(C3-ms)与受体数量少的细胞结合,而这些细胞用其他检测技术无法检测到。用抗CR1和抗CR2进行的抑制研究表明,C3b-ms和C3d-ms分别仅与CR1和CR2结合。制备C3-ms仅需要少量部分纯化 的C3,不需要免疫球蛋白或其他补体成分。一旦形成,C3-ms在4℃下可稳定保存长达4个月。