Reynolds G M, Rowlands D C, Mead G P
Department of Pathology, Medical School, University of Birmingham, Edgbaston.
J Clin Pathol. 1995 Dec;48(12):1138-40. doi: 10.1136/jcp.48.12.1138.
This report describes the characterisation of a polyclonal sheep antiserum against the Ki67 antigen. On western blots, this antiserum recognises a pair of bands of high molecular weight identical with those seen with another polyclonal Ki67 antiserum and the MIB 1 monoclonal antibody. The new antiserum showed nuclear staining of a proportion of cells in paraffin wax embedded tissue sections following antigen retrieval using a microwave oven or pressure cooker. This staining pattern was blocked by incubating the serum with the peptide used as immunogen. The proportion and distribution of immunostained nuclei was identical with that seen with the alternative reagents that recognise the Ki67 antigen. The new reagent stained the same proportion of cells when used over a wide range of dilutions. There was no cross-reactivity with unrelated antigens sometimes detected by the monoclonal antibodies.
本报告描述了一种针对Ki67抗原的多克隆绵羊抗血清的特性。在蛋白质免疫印迹法中,该抗血清识别出一对高分子量条带,与另一种多克隆Ki67抗血清和MIB 1单克隆抗体所识别的条带相同。在用微波炉或高压锅进行抗原修复后,新抗血清在石蜡包埋组织切片中显示出一定比例细胞的核染色。通过将血清与用作免疫原的肽一起孵育,这种染色模式被阻断。免疫染色细胞核的比例和分布与识别Ki67抗原的其他试剂所观察到的相同。当在广泛的稀释范围内使用时,新试剂染色的细胞比例相同。该试剂与单克隆抗体有时检测到的无关抗原没有交叉反应。