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作 者:韩庆安[1] 姜平[1] 董永毅 郝勤宗[2] 裘孝良[2] 班进林 陈溥言 蔡宝祥[1]
机构地区:[1]南京农业大学农业部动物疫病诊断与免疫重点实验室,江苏南京210095 [2]河北农业大学动物科技学院,河北保定071001
出 处:《中国兽医学报》2000年第2期145-147,共3页Chinese Journal of Veterinary Science
基 金:中华农业科教基金;江苏省"九五"重点攻关项目!( BE964 0 4)
摘 要:利用猪繁殖与呼吸道综合征病毒 ( PRRSV)国内分离株 J1 ,采用反复差速离心法制备免疫抗原 ,长程免疫法免疫 BALB/ c小鼠 ,用间接 ELISA方法检测抗体 ,通过细胞融合技术 ,并经 3次亚克隆获得了 1 0株能稳定分泌抗 PRRSV单抗的杂交瘤细胞克隆株 ( A1 D7H1 0 ,A1 D7H1 1 ,A1 E7H9,A1 E7D9,A2 D8E7,A2 D8B1 1 ,B3D1 1 D6 ,B3D1 1 E6 ,B2 G9A9,B2 G9F2 )。这些细胞经体外连续传代 1个月和冻存 2个月复苏后 ,均能稳定分泌高效价的抗 PRRSV抗体 ,并能在小鼠体内形成肿瘤 ,有效诱导产生高效价 PRRSV抗体腹水 ( ELISA效价为1 0 - 3~ 1 0 - 4 )。其中有 7株能与美洲弱毒株Indirect enzyme linked immunosorbent assay(ELISA) method was developed to detect antibodies against PRRSV with J 1 isolated from the Huabei region of China. The viral antigens were purified by a number of centrifugations at low speed and ultraspeed. After the BALB/c mice to be immunized five times,the secreting antibody hybridomas were obtained.By screening with ELISA and cloning three times using the method of limiting dilution,ten hybridoma cell lines with a high and stable level of antibodies secreted were developed. The monoclonal antibodies were produced in cell culture supernatants or in ascites. The ELISA titer of the ascites was 10 -3 10 -4 .Among them,seven hybridoma cell lines of monoclonal antibodies of PRRSV J 1 strain could be bound to Rerp PRRSV strain.
分 类 号:S858.282.4[农业科学—临床兽医学]
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