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陕北白绒山羊Lhx2基因cDNA序列的克隆与原核表达
引用本文:刘 敏,白丁平,耿荣庆,方 堃,陈玉林. 陕北白绒山羊Lhx2基因cDNA序列的克隆与原核表达[J]. 西北农业学报, 2012, 21(4): 1-5
作者姓名:刘 敏  白丁平  耿荣庆  方 堃  陈玉林
作者单位:西北农林科技大学 动物科技学院,陕西 杨凌,712100
基金项目:农业部转基因生物新品种培育科技重大专项,国家自然科学基金
摘    要:根据GenBank中已发表的Lhx2基因序列设计引物,采用RT-PCR方法,从陕北白绒山羊皮肤组织克隆Lhx2基因编码区cDNA,对其进行生物信息学分析,并构建原核表达载体pET-Lhx2,在大肠杆菌BL21(DE3)中表达。最终获得陕北白绒山羊Lhx2基因,长1 221bp;酶切和测序结果显示,原核表达载体pET-Lhx2构建成功;SDS-PAGE和Western blot分析表明,重组原核表达载体在大肠杆菌中成功表达出目的融合蛋白。

关 键 词:陕北白绒山羊  Lhx2  克隆  原核表达

Cloning and Prokaryotic Expression of Lhx2 Gene from Shaanbei White Cashmere Goat
LIU Min,BAI Dingping,GENG Rongqing,FANG Kun and CHEN Yulin. Cloning and Prokaryotic Expression of Lhx2 Gene from Shaanbei White Cashmere Goat[J]. Acta Agriculturae Boreali-occidentalis Sinica, 2012, 21(4): 1-5
Authors:LIU Min  BAI Dingping  GENG Rongqing  FANG Kun  CHEN Yulin
Affiliation:(College of Animal Science and Technology,Northwest A&F University,Yangling Shaanxi 712100,China)
Abstract:The cDNA of Lhx2 gene was amplified from the skin of Shaanbei White Cashmere Goat by RT-PCR using one pair of primers which was designed and synthesized according to the Lhx2 gene sequence in GenBank.The biological information analysis was performed with it.The prokaryotic expression vector pET-Lhx2 was constructed and expressed in E.coli BL21(DE3).The cDNA of Shaanbei White Cashmere Goat Lhx2 gene was 1 221 bp.Restriction enzyme mapping and sequencing showed that prokaryotic expression vector was constructed successfully.SDS-PAGE and Western blot showed that the recombinant prokaryotic expression vector expressed the fusion protein(65 ku)successfully.
Keywords:Shaanbei White Cashmere Goats  Lhx2  Cloning  Prokaryotic expression
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