摘要
以质粒ＰＢＲ３２２为载体、ＢａｍＨＩ部分酶切片段（４～１０ｋｂ）为目的片段成功构建了大鼠基因组文库并进行了鉴定，文库总重组子数为３．２×１０７，插入比例９５％，为大鼠ＡＰＫＤ基因的克隆筛选以及有关大鼠基因的其它一些研究奠定了基础．
The rat genome library which has PBR322 as vector and 4～10 kb DNA segments cut by BamHI restriction enzyme as aim segments has been successfully constructed and identified. This library has 3.2×10 7 recombinants and the insertion ratio is 95%, which is the foundation of rat APKD gene clone selection and some other research work obout rat gene.
出处
《西南民族学院学报（自然科学版）》
CAS
1998年第1期42-47,共6页
Journal of Southwest Nationalities College(Natural Science Edition)
