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重组基因的英文

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"重组基因"怎么读用"重组基因"造句

英文翻译手机手机版

  • rec gene
  • recombination gene

例句与用法

  • Genetic material produced by gene - splicing
    重组基因材料基因分割而产生的基因材料
  • Present research on the sub - cell localization of expression product of exogenous recombination gene
    外源重组基因表达产物亚细胞定位的研究现状
  • Recombination gene was cut - down and introduced into the nuclei of oocytes or the cytoplasm of goldfish at one - cell stage via microinjection . the results as follows : ( 1 ) fluorescence was observed from embryo under suitable uv light after microinjection 36 hours . the fluorescent ratio of gastrula embryo period was up to 25 %
    采用显微注射法将这种重组基因转化1细胞期的金鱼受精卵,实验结果如下: ( 1 )显微注射后,根据胚胎发育分期,胚胎在显微注射后36小时开始能在紫外灯下观察到荧光,原肠期发荧光的胚胎比例为25 ,后期发育荧光率逐渐下降,肌肉效应期后又相对稳定。
  • There are a variety of mechanisms believed to be involved , including genomic modularity - - the ability for animals to reorganize their genome in response to stress or other outside influence , heterozygous fractionation ( heterozygous genes in parents can lead to speciation by having multiple homozygous genes in children ) , and standard evolution
    认为涉及很复杂的变化机制-动物重组基因组响应压力或其它外在影响的能力(双亲基因杂交会导致孩子们拥有许多纯合子基因的物种形成) ,而标准地进化。
  • The interesting gene fragment with ecori and noti were amplified by overlapping pcr , which inserted into vector plasmid ppic9k after degisted by ecori and noti , and the recombinant plasmid was transformed into competent dh5cc . positive clones were screened by pcr from the lb plate with amp . digesting analysis resulte shows that the interesting gene were inserted into the vector ppic9k with correct direction
    目的基因经双酶切后连接载体ppic9k ,然后导入大肠杆菌dh5中,在含氨卞青霉素( amp )的lb板上用pcr反应筛选出阳性菌落,双酶切结果表明目的基因已插入载体中,且方向正确,测序结果进一步证明人巨细胞病毒重组基因表达质粒成功地克隆了目的基因片段。
  • In order to express alkaline protease gene ( ap gene ) in bacillus subtil is , the recombinant expression plasmid was constructed . this plasmid contains a promoter bp53 , also from b . pumilus un - 31 - c - 42 , ap gene and the shuttle vector psugv4 . after introduced into b . subtilis wb600 , the transformants displayed the hydrolyzed zone on milk plate
    将来自短小芽抱杆菌un一31一c礴2的基因启动子( bp53片段)和脱毛蛋白酶全基因( ap )进行融合,然后将重组基因(命名为bpap )插入到大肠杆菌-枯草杆菌穿梭质粒载体psugv4中,构建成表达质粒psu一bpap 。
  • The recombination gene micyoinjected is 5nl dna ( about 106 - 107 ) into everyone oocytes or cytoplasm of grass carp . there were 32197 oocytes of 12 series via micyoinjection and achived 12945 fries in 2000 year , by hatching and raising . genomic dna was extracted from grass carp who were transformated in 1120 grass carp presented postive reaction by blood
    实验通过将hu - - ifn基因重组分子采用显微注射法将这种重组基因转化草鱼1 - 2细胞期的受精卵,即以narashige显微注射仪,将5nldna (约10 ~ 6 10 ~ 7分子)直接注射到选择好的受精卵核的动物极上。
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