Sidberry H, Kaufman B, Wright D C, Sadoff J
J Immunol Methods. 1985 Feb 11;76(2):299-305. doi: 10.1016/0022-1759(85)90307-2.
A rapid, sensitive immunoenzymatic technique for the analysis of lipopolysaccharide (LPS) from gram-negative bacteria using monoclonal antibodies is described. After separation by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the LPS was either stained with silver or electrophoretically transferred to nitrocellulose. After reaction with anti-LPS monoclonal antibodies, the transferred antigens were visualized by reaction with alkaline-phosphatase-labelled anti-mouse antibodies and a substrate containing naphthol phosphoric acid and Fast Red.
描述了一种使用单克隆抗体分析革兰氏阴性菌脂多糖(LPS)的快速、灵敏的免疫酶技术。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离后,LPS 可用银染色或电泳转移至硝酸纤维素膜上。与抗 LPS 单克隆抗体反应后,通过与碱性磷酸酶标记的抗小鼠抗体及含有萘酚磷酸和固红的底物反应来显示转移的抗原。