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起始位点的英文

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"起始位点"怎么读用"起始位点"造句

英文翻译手机手机版

  • initiation site

例句与用法

  • Using ribosome scanning model to predict translation initiation sites
    用核糖体扫描模型预测翻译起始位点
  • Tis , translation initiation site
    真核生物翻译起始位点
  • Computational location of transcription start sites in prokaryotic genome based on sliding window
    基于滑动窗口的原核转录起始位点计算定位方法
  • By artificially changing a to c at - 137 bp site upstream from transcription start point of cloned promoter , two site - mutation promoters , ipms ( 603 bp ) and ipm1 ( 900 bp ) were created
    通过pcr方法对克隆的两个启动子进行定点突变,使转录起始位点上游- 137bp处a突变为c ,得到两个突变启动子( ipml 、 ipms ) 。
  • Uppsala university scientists have discovered an entirely new process in which short , tiny " antisense rna " competes with the protein - producing ribosomes for starting sites for reading messenger rna
    乌普萨那大学的科学家们发现了一个全新的进程,在短期内,微小的“反义核糖核酸”具有与制造蛋白质的核糖体竞争信使rna起始位点的能力。
  • Activity of each construct was determined . the basal promoter was located at about 60bp up stream of the transcription initiation site . it contains a tata box at - 33bp which is required for the transcription initiation
    基因的基本启动子元件位于转录起始位点上游约60bp ,其中含有一个位于- 33bp处的tatabox ,它对于转录起始起着重要作用。
  • 900 bp promoter - directed gus expression was highly induced by sa and bth , while the 603 bp promoter , whether mutated or not , did not respond to sa and bth induction , which indicated that the element in response to sa and bth lied among 575 ~ 872 bp from transcription start site
    全长900bp启动子能够应答sa和bth的诱导,而603bp长的启动子无论突变与否对sa和bth均无应答,证明sa和bth的应答区域在克隆启动子的转录起始位点上游575 872bp之间。
  • The pa7 fragment was sequenced and several motifs similar to prokaryotic promoter elements such as - lobox , - 35box and up box were found . the sd sequence which was bound by ribosome and atg site were also found . the pat fragment was blast in genebank , but there is no its " homological sequence
    对pa7片段的序列分析发现其距5 ’端931bp ? 1091bp处具有原核生物典型基因启动子的保守结构- 10区和- 35区,以及翻译必需的sd序列和翻译起始位点等。
  • In order to use the responding ability to the inducers of pr - la promoter , two fragments , ip1 ( 900 bp ) and ips ( 603 bp ) were cloned from tobacco genomic dna by polymerase chain reaction ( pcr ) with primers designed according to the sequence reported in genbank . sequence analysis of the amplified 900 bp fragment indicated that the cloned sequence had 99 % of homology to the known sequence . its transcription start site , tata box and consensus sequence " tgac " conserved in pr genes were identical to those of pr - la promoter
    根据pr - 1a基因的报道序列,设计两对引物,以烟草基因组为模板,通过pcr扩增得到900bp ( ipl )和603bp ( ips )两个目标片段,序列测定表明克隆的启动子与报道序列具有99的同源性,转录起始位点、 tatabox及保守序列tgac与报道序列均完全相同。
  • The entire halcs gene is located on a megaplasmid and contains a 849 - bp open reading frame that encodes a polypeptide of 283 amino acids . the promoter is typically haloarchaeal , but the start site of transcription is only seven bases from the 5 ' end of the initiator aug codon , making the halcs transcript another example of a " leadless transcript " in the haloarchaea
    它的一29一24位置上是一“毛幻人” box序列,为典型的嗜盐古菌启动子;它的转录起始位点距离“ atg ”只有7个核普酸,也是典型的嗜盐古菌的“卜adless腼script ’ ’ 。
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