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操纵子基因的英文

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"操纵子基因"怎么读用"操纵子基因"造句

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  • operon gene

例句与用法

  • Then the engineered genes of bio operon were carried on testing of the functional expression , and biow & biob gene were induced to express
    而后对改造后的生物素操纵子基因进行了功能表达检测及biow与biob基因的诱导表达。
  • Used as 1 . 1094 strain of bacillus subtilis as researched material , the structural genes of biotin operon ( bio operon ) were cloned , and its sequence were engineered
    本研究以枯草杆菌asl . 1094菌株为研究材料,克隆了生物素操纵子基因,并对基因序列进行改造。
  • This experiment probed how to improve the expression efficiency of the structural genes of bio operon , and provided the feasibly researched route and scientifically theoretical foundation
    旨在探索如何提高生物素操纵子基因的表达效率,为该操纵子基因的高效表达提供可行的研究路线和理论依据。
  • Used the genomic dna extracted by low melting - point agarose embedding method as pcr template , the full length of structural genes of bacillus subtilis bio operon were gained by long pcr method
    将该方法提取的基因组dna稀释100倍作为模板,采用长距离pcr方法,获得了枯草杆菌生物素操纵子基因全长。
  • Contrasting analysis with the genes sequence of bacillus subtilis 168 strain ' s bio operon , the sequence of bio operon of as 1 . 1094 strain had 12 bases difference with that of 168 train , and 7 bases caused variation of amino acid
    1094菌株与168菌株bioafdb基因序列完全一致, 9个差异碱基是由于pcr扩增导致的。枯草杆菌生物素操纵子基因4个亚克隆序列的测序结果证实, asi
  • 2 . cloning of structural genes of bacillus subtilis bio operon diluted the genomic dna of bacillus subtilis as the template , long pcr product ( 10 . 3kb ) and three salvage pcr products were separately gained by optimization of reaction conditions of pcr
    枯草杆菌生物素操纵子基因的克隆将枯草杆菌基因组dna稀释后,通过pcr反应条件的优化,分别扩增得到了生物素操纵子基因的长距离pcr产物( 10 . 3kb )和3个分段pcr产物。
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