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cloning dna中文是什么意思

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用"cloning dna"造句"cloning dna"怎么读"cloning dna" in a sentence

中文翻译手机手机版

  • 克隆dna

例句与用法

  • A bt - e . coli shuttle vector pht315 was deleted its replication region of bt , then constructed a novel vector named pht315 - 1 which composed a multiple cloning site , erythromycin and ampicillin - resistance marker and could only replicated in e . coli . used pht315 - 1 , a 5273 bps dna fragment carrying a novel bt plasmid replicon was isolated and registered in genbank as ay278324 . sequence analysis showed that there were at least three orf ( open reading frame ) in the cloned dna encoding 501 , 333 , 183aas . orfl had 98 % identities with replicating related protein ori43 of bt strain hd263 . the others were no homology to any published bt replicating related protein . after continuous cultured for 70h at 30 c without antibiotic selecting press . the stability of plasmid carrying cloned replicon in bt acrystalliferous mutant strain hd73 cry was more than 98 % . and growth curve also showed that the novel replicon was stable and could replicate normally
    进一步序列分析表明该复制区至少有3个较大的orf ,分别编码501 , 333 , 183个氨基酸。其中orf1蛋白序列与hd263复制蛋白ori43的同源性为98 ,而另外两个orf和genbank己公布的bt复制相关蛋白无同源性。 30连续培养72h ,复制区质粒在bt无晶体突变株hd73cry ~ -中稳定性达98以上, 30h生长曲线也表明该复制区能够在bt中稳定复制和遗传,对受体菌株无明显不良影响。
  • After enzyme restriction and sequencing analysis , the nucleotide data had been further analyzed by antheprot 5 . 0 and clutalw softwares . the analysis results showed that the cloned dna fragment had a longest open reading frame ( orf ) of 1035nt , it predicted to be encoded a 344 - aa protein with the molecular weight of 36kda
    应用antheprot5 . 0 、 clustalw等分子生物学软件分析,显示主要外膜蛋白前24个氨基酸是较强的疏水性区域,可组成信号肽,其与omp基因的同源率达96 ,氨基酸的同源率高达98 。
  • To prove that the cloned dna fragment can express tryptopanase , a new plasmid pet28c - tnaa , in which the cloned dna fragment was located downstream of t7 promoter on pet28c was constructed and transformed into host bl21 ( de3 ) , a bl21 lysogen of bacteriophage de3 in which the only promoter known to direct transcription of the t7 rna polymerase gene is the lacuvs promoter , which is inducible by iptg
    用iptg诱导表达t7rna聚合酶,以表达质粒上的目的基因。在葡萄糖存在的条件下,用常规方法发酵和诱导( 37 1mmiptg ) ,发现表达的蛋白质条带的分子量与理论上计算的分子量一致。但是发酵液中检测不到吲哚,表明虽然表达了目标蛋白,但表达的蛋白质没有酶活性。
用"cloning dna"造句  

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