论文部分内容阅读
为了制备抗重组人孕激素受体单克隆抗体,用聚合酶链反应(PCR)扩增人孕激素受体氨基端编码区段,定位克隆连入高效表达载体PMS-31b,构建重组质粒PMS-PRa,将其转入大肠杆菌POP2136,经30℃扩增和42℃温度诱导,表达出分子量为33kD的MS2-PRa融合蛋白。摇菌液的蛋白表达量约为30mg/L。用这种蛋白免疫BALB/c小鼠,制备出4株抗人孕激素受体的单克隆抗体。它们用于乳腺癌石蜡和冰冻切片的免疫组织化学染色,较国外制备的单克隆抗体质量更好
In order to prepare anti-recombinant human progestin receptor monoclonal antibody, the coding region of human progesterone receptor was amplified by polymerase chain reaction (PCR), and inserted into the high expression vector PMS-31b to construct the recombinant plasmid PMS- PRa was transformed into E.coli POP2136. After induced by temperature 30 ℃ and temperature 42 ℃, MS2-PRa fusion protein with a molecular weight of 33 kD was expressed. Vibrio fungus protein expression of about 30mg / L. BALB / c mice were immunized with this protein to prepare 4 monoclonal antibodies against human progesterone receptor. They are used for immunohistochemical staining of paraffin and frozen sections of breast cancer and are of better quality than monoclonal antibodies prepared abroad