consensus sequence造句

• To correlate microarray data with the promoter site consensus sequence for a specific transcription factor
  找出微阵列资料与特定转录因子的促进子共识序列之间的相互关联性。
• The other 15 peptides were classified into 2 groups , each group sharing a different consensus sequence that might bind a different site of the target . one peptide of each group was chemically synthesized and added to the rdrp reaction system . we found that one peptide refrained the activity of rdrp
  自2组结合肤中各选择1个环肤分子用化学方法合成，将合成肤加入rdrp反应体系后，其中1个环肤分子对rdrp活性表现明显的拮抗作用，加入细胞培养中可对den感染细胞产生明显的保护作用。
• 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。
• In this dissertation , the following experiments are conducted : firstly , cloning of hpab - gene , i ) the amino acids sequences of 23 animal - peptide antibiotics were analyzed by multiple sequences alignment method and a pair of degenerated primers were designed according to the consensus sequence derived from mature peptides of some beta peptide antibiotics
  人源肽抗生素hpab -的基因克隆：对动物23种型肽抗生素的氨基酸序列进行对比，选择部分相似性较高的序列，分析其成熟肽的结构特点，抽提型肽抗生素的一级结构特征，并以此为基础设计简并引物。
• But polyadenylation in bacteria needs no specific consensus sequence or there is no such sequence signals found . the sites of polyadenylation of bacterial mrna are diverse , including the 3 ' ends of primary transcripts , the sites of endonucleolytic processing in the 3 ' untranslatd and intercistronic regions , and sites within the coding regions of mrna degradation products
  细菌mrna多聚腺苷酸化的位点多种多样，包括初级转录产物的3 ’末端， 3 ’端非翻译区和顺反子间区的内切酶加工位点及mrna降解产物的编码区内，其腺苷酸化相对无特异性、无选择性。
• In the part i , the sequence of the cloned promoter osg6b " was first analyzed . osg6b " had a whole length of 1688 bp and 98 % homology to known sequence of promoter osg6b . its transcriptional start point , tata boxes and the consensus sequences " tgtgg " conserved usually in anther - specific promoters were identical to those of reported osg6b
  第一部分：对已克隆的启动子osg6b ’进行的序列分析表明， osg6b ’全长1688bp ，与报道的osg6b有98的同源性，两者在转录起始位点、 tatabox及其它花药特异性启动子共有的保守序列tgtgg完全相同。