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1)  Homologous recombination
同源重组
1.
Construction of cDNA library from mouse oocyte for yeast-2-hybrid system by homologous recombination;
同源重组法构建小鼠卵母细胞cDNA酵母双杂交文库的探索
2.
Construction of CHO high expression cell line by means of homologous recombination;
利用同源重组建立CHO高表达细胞株
3.
Construction of recombinant adeno-viral plasmid bearing hSDF-1α cDNA by homologous recombination in bac-teria and preparation of recombinant adenovirus expressing hSDF-1α;
细菌内同源重组快速构建和制备表达hSDF-1α的重组腺病毒
2)  homogenous recombination
同源重组
1.
Then pDC316-BMP-7 and the framework plasmid pBHGlox_E1,3Cre were transfected into HEK293 cells for homogenous recombination in cells with Lipofectamine 2000.
方法用基因工程技术将人BMP-7基因cDNA亚克隆至穿梭质粒pDC316上,利用脂质体介导的方法将AdMax腺病毒包装系统的骨架质粒pBHGlox_E1,3Cre和穿梭质粒pDC316-BMP-7转染入HEK293细胞,进行同源重组,得到腺病毒重组质粒Ad5-BMP-7,并在其中包装扩增病毒。
2.
Methods The human HIF-1α gene fragment was cloned into the shuttle plasmid pAdTrack-CMV to form the transfer vector by the method of homogenous recombination in bacteria, and then was transfected into HEK293 cells with Lipofectamine TM 2000.
方法采用基因工程技术,经过亚克隆将人HIF-1α基因片段克隆至穿梭质粒pAdTrack-CMV上,利用pAdEasy系统进行细菌内同源重组后,经脂质体转染HEK293细胞,进行重组腺病毒的包装、扩增。
3.
Methods The human p16 gene fragment was cloned into the shuttle plasmid pAdTrack-CMV to form the transfer vector by the method of homogenous recombination in bacteria.
方法用基因工程技术将人p16基因cDNA亚克隆至穿梭质粒pAdTrack-CMV上,利用PAdEasy系统进行细菌内同源重组,然后通过脂质体将正确重组体包裹并转染293T细胞,并在其中包装扩增病毒。
3)  homologous recombinant
同源重组
4)  DNA homologous recombination
DNA同源重组
5)  Red recombination
Red同源重组
1.
The Escherichia coli strain SQ88 was selected as the target strain,to which five of rRNA operons(rrnA,rrnD,rrnE,rrnG and rrnH)were sequentially inactivated using λ Red recombination system.
以1株染色体上的5个rRNA操纵元(rrnA、rrnD、rrnE、rrnG和rrnH)被敲除的大肠杆菌(Escherichia coli)菌株SQ88为出发菌,运用λRed同源重组系统和卡那霉素抗性基因筛选重组子,并利用抗性基因两端的FRT位点通过位点专一性重组将抗性基因去除,最终成功构建了1株仅具有单拷贝rRNA操纵元(rrnB)的E。
6)  λ Red recombination system
λRed同源重组
补充资料:同源重组技术
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