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作 者:宋晓彤[1] 冯振卿[1] 仇镇宁[1] 李芸茜[1] 林敏[2] 柏慧 沙家豪[2] 管晓虹[1]
机构地区:[1]南京医科大学医学分子生物研究所,南京210029 [2]南京医科大学生殖医学研究中心
出 处:《中国血吸虫病防治杂志》2002年第1期11-13,共3页Chinese Journal of Schistosomiasis Control
基 金:国家自然科学基金 ( 39970 6 70 )
摘 要:目的 分离日本血吸虫单克隆抗独特型抗体 NP30重链可变区 (VH)基因并测定其序列。方法 根据鼠免疫球蛋白重链可变区基因 FR1和 FR4序列的保守性 ,化学合成体外扩增 Ig重链可变区基因的数对引物。以日本血吸虫单克隆抗独特型抗体 NP30的杂交瘤细胞株基因组 DNA为模板 ,扩增 VH 基因 ,将其克隆入 p U C19载体 ,重组子用 Sanger's双脱氧链终止法测定序列 ,将序列与Gene Bank中已发表的抗体序列比较。结果 VH 基因全长 35 7bp,属鼠免疫球蛋白重链第 亚类 ,由种系基因 V、Dsp2 .8与 JH4重排而来。该 VH 基因序列已被 Gene Bank收录 (accession NoAF2 82 6 2 2 )。结论 该 VH 基因为日本血吸虫单克隆抗独特型抗体Objective To amplify and sequence the heavy chain of anti idiotypic monoclonal antibody NP30 of Schistosoma japonicum. Methods By comparing the conserved regions at each end of the nucleotide sequences of murine germ line genes encoding FR1 and FR4 regions of immunoglobulin heavy chain variable regions, a set of primers for amplification of V H gene were designed. The hybridoma cells secreting anti idiotypic monoclonal antibody NP30 of Schistosoma japonicum were cultured and their genome DNA was extracted and used as template for PCR. The PCR product was then cloned into pUC19 vector. The recombinants were sequenced by Sanger's method. The V H gene was compared with Gene Bank and published mouse V H genes. Results It was proved that a full length V H gene was 357 bp, and a member of mouse Ig heavy chain subgroup Ⅱand originated from rearrangement of germ line V?Dsp2 8 and J H4 genes. The V H gene sequence was registered by Gene Bank (accession No. AF282622). Conclusions It was suggested that obtained V H gene was potentially functional gene of anti idiotypic monoclonal antibody NP30 of Schistosoma japonicum.
关 键 词:日本血吸虫 抗独特型抗体 单克隆抗体 基因扩增 序列分析 NP30 重链可变区
分 类 号:R383.24[医药卫生—医学寄生虫学] R392-33[医药卫生—基础医学]
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