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作 者:隋拥君[1] 丁广治[1] 唐佩弦[1] 侯春梅[1] 毛宁[1]
机构地区:[1]军事医学科学院基础医学研究所
出 处:《免疫学杂志》1997年第3期164-167,共4页Immunological Journal
摘 要:应用RT-PCR技术从人B淋巴瘤细胞系Raji中克隆到B7-1(CD80)cDNA,并经测序证实。将其插入至真核表达载体pLXSN中,用脂质体转染小鼠黑色素瘤细胞B16,G418筛选,并经流式细胞仪检测,得到了细胞表面表达B7-1的重组克隆。PCR从其基因组DNA中扩增到B7-1基因,提示B7-1cDNA已整合至宿主细胞的基因组DNA中。本文为研究B7-1在肿瘤免疫中所起的作用奠定了基础。B7 1(CD80) cDNA was cloned by RT PCR from human B lymphma Raji cell line and confirmed by DNA sequencing.The recombinant expressing vector was constructed by inserting the B7 1 cDNA into pLXSN vector.After transfecting by lipofectamine and selecting with G418,the B7 1 transfected recombinant clone was obtained.It was confirmed that the B7 1 cDNA had been integrated into the genomic DNA of B16 B7 cells by PCR analysis.Our study enables us to further investigate the role of B7 1 in tumor immunotherapy.
关 键 词:B7-1(CD80) 基因克隆 基因表达 黑色素瘤
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