Nakazawa N, Maki K, Ogawa H, Ikeda O, Sakagami M
Radioisotopes. 1977 May;26(5):291-5. doi: 10.3769/radioisotopes.26.5_291.
The antisera using at final dilution of 1 : 10,000 have been prepared by immunizing synthetic human proinsulin connecting peptide to rabbits for human proinsulin C-peptide radioimmunoassay. The cross reactivities of human proinsulin C-peptide derivatives with the prepared antisera were reduced by leaving amino acid residues from N terminal, although this phenomenon was a little different among antisera. Those results suggested that main antigen determinant in N terminal 31-38 of human proinsulin connecting peptide. The cross reactivities of other animal proinsulin C-peptide and other peptide hormones with the prepared antissera were not recognized at 10(3) p mole/ml.
已通过用合成人胰岛素原连接肽免疫兔子来制备用于人胰岛素原C肽放射免疫测定的抗血清,其终稀释度为1:10000。通过从N端去除氨基酸残基,人胰岛素原C肽衍生物与所制备抗血清的交叉反应性降低,尽管这种现象在不同抗血清之间略有不同。这些结果表明人胰岛素原连接肽N端31 - 38中的主要抗原决定簇。在所制备的抗血清中,10³ p摩尔/毫升时未检测到其他动物胰岛素原C肽和其他肽类激素的交叉反应性。