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牛分枝杆菌RecA基因的克隆与序列分析
引用本文:王春芳,郭伟生,姜秀云,钱爱东.牛分枝杆菌RecA基因的克隆与序列分析[J].湖北农业科学,2009,48(10).
作者姓名:王春芳  郭伟生  姜秀云  钱爱东
作者单位:1. 吉林农业大学,动物科技学院,长春,130118
2. 吉林农业大学,生命科学学院,长春,130118
基金项目:国家科技支撑计划项目 
摘    要:以牛分枝杆菌(Mycobacterium bovis)Valleelll株染色体DNA为模板,以RecA基因特异性引物进行PCR扩增,获得约240 bp的DNA片段.将PCR产物克隆至pMDTM18-T Vector中,通过α-互补法筛选、质粒PCR鉴定及序列分析鉴定,成功构建出了重组质粒pMDTM18-T-RecA,为进一步研究RecA基因及其在牛结核病诊断中的应用奠定了基础.

关 键 词:牛分枝杆菌  RecA基因  克隆  序列分析

Cloning and Sequential Analysis of Mycobacterium bovis RecA Gene
WANG Chun-fang,GUO Wei-sheng,JIANG Xiu-yun,QIAN Ai-dong.Cloning and Sequential Analysis of Mycobacterium bovis RecA Gene[J].Hubei Agricultural Sciences,2009,48(10).
Authors:WANG Chun-fang  GUO Wei-sheng  JIANG Xiu-yun  QIAN Ai-dong
Abstract:The chromosome DNA was extracted from Mycobacterium bovis Valleelll,the RecA gene was amplified with a pair of specific primers by using polymerase chain reaction (PCR). The PCR product was approximately 240 bp DNA segment. The PCR product was cloned into pMD?8-T Vector,then by using a-complementation test,PCR assay and recom-binant plasmid sequential analysis,recombinant plasmid pMD?8-T-RecA was successfully constructed. These results could serve as a solid basis for further studies on the usefulness of RecA gene and its application in diagnosis of tuberculosis.
Keywords:Mycobacterium bovis  RecA gene  cloning  sequential analysis
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