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机构地区:[1]新乡医学院细胞生物学教研室,新乡453003 [2]河南师范大学生命科学学院,新乡453002
出 处:《遗传》2004年第6期793-796,共4页Hereditas(Beijing)
基 金:国家自然科学基金 (No .3 9970 3 62 );河南省重大科技攻关项目 (No .0 12 2 0 3 190 0 )资助~~
摘 要:抽提常氏肝癌细胞的总RNA ,以oligo(dT)为引物 ,通过两次转换模板 ,采用LD PCR合成全长cDNA ,在cDNA两端引入SfiⅠ的酶切位点。以λTriplEX2为载体经过包装后构建了常氏肝癌细胞cDNA表达文库。以ADAMs通用抗体 ,用免疫筛选技术从常氏肝癌cDNA文库中筛选出 2 2个阳性克隆 ,经测序分析和BLAST检索 ,证实其中一个为新基因 ,部分区域具有蛋白酶的功能 ,对该基因进行了GenBank登录 ,获注册号为AY0 780 70。Total RNA was isolated from Chang Liver cell. The full-length cDNA was synthesized using LD PCR by RNA 5′ end switching mechanism,oligo(dT) as primer. SfiⅠ digestion sites were introduced at both 3′ and 5′ end of cDNA. The cDNA was ligated with λTriplEX2 vector and packaged. Twenty-two positive clones were obtained by immunoscreening to the library,they were sequenced and blast in NCBI,one of them was identified a novel gene. It was submitted to GenBank and obtained accession nubmer AY078070. It may lay down a foundation for studying on functions of ADAMs related gene.
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