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switch gene
相关语句
  开关基因
     Studies on the DNA Repair Switch Gene pprI of Deinococcus Radiodurans
     耐辐射球菌DNA修复开关基因pprI的研究
短句来源
     Do RT-PCR for TGF- β 2, CTGF、 G0/G1 switch gene 2, make sure how they work in the early stage of the wound healing.
     收集正常时及伤后6h,24h,72h的小鼠角膜,行RT-PCR,观察TGF-β2、CTGF、G0/G1开关基因2的变化,该实验同时是对基因芯片数据的验证。
短句来源
     TGF-β2、 CTGF and G0/G1 switch gene2 go a temporary upregulation but down to normal level in 72 hours, the same as the 72h microarray show.
     3.TGF-β2、CTGF、G0/G1开关基因2在伤后24h一过性增高,之后下调。
短句来源
     The Deinococcus radiodurnas pprI, a switch gene responsible for DNA repair, was transformed to E. coli via a shuttle plasmid pRADZ3 and a recombinant fusion PprI protein was expressed in normal growth condition without induction. The stable expression of PprI protein in E.
     将耐辐射球菌 (Deinococcusradiodurans)与DNA修复有关的开关基因—pprI通过穿梭质粒pRADZ3导入大肠杆菌TG1中 ,使其在正常培养条件下 (不需诱导剂 )表达PprI蛋白 ,并通过Westernblot证实该基因在TG1中可稳定表达。
短句来源
  “switch gene”译为未确定词的双语例句
     The optimal timing for intervene TGF- β2、 CTGF and G0/G1 switch gene must be in 24h post-injury.
     3.TGF-β2、CTGF的干预时机应在伤后24h内。
短句来源
  相似匹配句对
     Promoter is the gene switch for foreign genes expressing in plants.
     启动子是调控外源基因在植物体内表达的“开关”。
短句来源
     Studies on the DNA Repair Switch Gene pprI of Deinococcus Radiodurans
     耐辐射球菌DNA修复开关基因pprI的研究
短句来源
     GENE IMMUNITY
     基因免疫
短句来源
     KILL SWITCH
     杀戮开关
短句来源
     On Gene Patenting
     基因的专利问题
短句来源
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  switch gene
One of these may be involved in a switch gene repair operated control of recombination.
      
Sex-specific regulation of Md-dsx is controlled by the switch gene F via a splicing mechanism that is similar but in some relevant aspects different from that in Drosophila.
      
The secondquestion is evolutionary, concerned with understanding how a major develop mental switch gene like tru-1 changes with time and speciation.
      
This evidence suggests that C\EBP may indeed be the master-switch gene for the liver-to-pancreas transdifferentiation.
      
This latter mechanism operates in nodules and involves the cell cycle switch gene ccs52A.
      
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The Deinococcus radiodurnas pprI, a switch gene responsible for DNA repair, was transformed to E.coli via a shuttle plasmid pRADZ3 and a recombinant fusion PprI protein was expressed in normal growth condition without induction. The stable expression of PprI protein in E.coli TG1 was confirmed by Western blot. Empty plasmid pRADZ3 was transformed to E.coli TG1 as control. The viabilities under H 2O 2 oxidative stress and the differences in catalases(KatE, KatG) activities of these two reconstructed E.coli...

The Deinococcus radiodurnas pprI, a switch gene responsible for DNA repair, was transformed to E.coli via a shuttle plasmid pRADZ3 and a recombinant fusion PprI protein was expressed in normal growth condition without induction. The stable expression of PprI protein in E.coli TG1 was confirmed by Western blot. Empty plasmid pRADZ3 was transformed to E.coli TG1 as control. The viabilities under H 2O 2 oxidative stress and the differences in catalases(KatE, KatG) activities of these two reconstructed E.coli TG1 were observed. The results showed that either in exponential phase or stationary phase, the expression of PprI protein in E.coli TG1 can enhance the viabilities, compared with the relative control; The results obtained from the Native-PAGE indicates that the expression of pprI in E.coli TG1 can enhance the enzymatic activity.It is concluded that the expression of D. radiodurans pprI can enhance the antioxidation in E.coli.

将耐辐射球菌 (Deinococcusradiodurans)与DNA修复有关的开关基因—pprI通过穿梭质粒pRADZ3导入大肠杆菌TG1中 ,使其在正常培养条件下 (不需诱导剂 )表达PprI蛋白 ,并通过Westernblot证实该基因在TG1中可稳定表达。与转化了空白质粒pRADZ3TG1对照 ,观察了改造后的两种大肠杆菌在有H2 O2 氧化压力下的存活率和大肠杆菌中两种过氧化氢酶 (KatE ,KatG)的活性表达差异。结果表明 ,无论在指数生长期还是稳定生长期 ,能表达PprI蛋白的大肠杆菌比对照的存活率要高出 1 0 %左右 ;非变性电泳结果表明 ,耐辐射球菌pprI在大肠杆菌中的表达使得KatE活性在指数生长期与稳定生长期分别增加 1 5~ 2倍和 2 5~ 3倍。证明耐辐射球菌pprI在大肠杆菌中的表达能够增强细胞抗氧化能力

 
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