摘要
将牛18ku-bFGF基因全编码序列插入质粒pEGFP-N1中,构建真核表达载体pCMV-bFGF,并用菌落PCR、酶切和测序等方法对重组质粒进行了鉴定。研究结果表明,检测结果均一致于预期,表明牛18ku-bFGF基因全编码序列已正确插入到载体中。
To further investigate functions of basic fibroblast growth factor(bFGF),bovine 18ku-bFGF gene was inserted into plasmid pEGFP-N1 to construct eukaryotic expressional vector pCMV-bFGF.The recombinant DNA was identified with colony polymerase chain reaction,digestion with restriction endonucleases and DNA sequencing to be a right insertion of the target gene into the digested plasmid pEGFP-N1 with the two same restriction endonucleases,which indicated that recombinant eukaryotic expressional vector was constructed successfully.
出处
《广东农业科学》
CAS
CSCD
北大核心
2012年第20期142-144,共3页
Guangdong Agricultural Sciences
基金
广西自然科学基金(0991011)
农业部水牛遗传繁育技术重点实验室开放基金(SNKF-2011-02)
关键词
牛18ku-bFGF
真核表达载体
构建
鉴定
bovine 18ku-bFGF
eukaryotic expressional vector
construction
identification