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coding sequence中文是什么意思

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  • The recombinant transfer vector pbacpak - hbmp was constructed by insertion of the hbmp coding sequences into the multiple cloning site of transfer vector pbacpak . 8 . bmn cell line was co - transfected with pbacpak - hbmp plasmid and linearized baculovirus bacpak6 dna by dosper agent
    将克隆到的hbmp基因通过适当的酶切插入到转移载体质粒pbac - pak8的多克隆位点中,获得重组转移载体质粒pbacpak - hbmp 。
  • Based on the single cycle detector , the finite cycle detector is proposed for the detection of phase - coded signals . the finite cycle detector has a good performance under unknown the spreading code sequence , initial phase , spreading code timing epoch
    针对相位编码信号的检测,提出了基于单循环检测器的有限多循环检测器,可在没有编码序列、初相、编码序列初始时间等信息的情况下,取得理想的检测效果。
  • On the basis of the composition of a file , the sequence of significant code sequences or based on particular behavior patterns , the heuristics can determine with a high probability whether it is dealing with a harmful or virulent file
    在文件的基层结构(不知道怎么翻译- _ - | | ) ,有意义代码的顺序或者基于特殊的行为特征(还是不知道怎么翻译- _ - | | ) ,有很高的几率可以启发出文件是否是一个有害的或者含有病毒的文件。
  • Every class endues a binary code , then a set of svms are used to solve the multiple binary problems . the generalization performance of ecc - svm is analyzed , which is determined by code length , hamming distance , coding sequence and margins of svms
    本文提出了基于纠错编码的svm多类分类算法( ecc - svm ) ,并分析了ecc - svm的推广能力与编码长度、码间汉明距离、编码顺序以及分类间隙等之间的关系,给出了这种关系的数学描述。
  • Fasl - ecd coding sequence is subcloned into pet - lla expressing vector , recombinant expression vector are named as pet - fasl - ecd . this plasmid is introduced into e . coli bl21 . after induction with 1mmol / l iptg , the protein expression is analyzed and confirmed by coomassie - stained sds - page
    用pcr和酶切鉴定的方法筛选出阳性重组子,将阳性重组子以ilnlnol几iptg进行诱导表达,以sds一page分析fasl胞外区的表达。
  • A 12 bp sequence of the 5 " end from the polyhedrin protein gene of bmnpv was ligated to the 5 ' end of hbsag ( pres2 + s ) protein coding sequence by pcr . the fusion product coding for hbv surface antigen medium sized ( hbmp ) with 4 - additional aa of bmnpv polyhedrin protein was obtained
    本研究通过pcr突变的方法,在hbsag ( pres2 + s )前s2序列的5 ’端融合了bmnpv多角体蛋白基因5 ’端的12个碱基,获得了融合乙肝表面抗原中蛋白基因( hbmp ) 。
  • The nj map and simplest principle map based on 3 ' end coding sequences are identical to the two maps based on the complete coding sequences . this shows that 3 " end coding sequences of epsp can replace the complete coding sequences to analyze the molecular evolution
    用epsps基因全长编码区的dna序列构建的nj图,最简约树与用其3 ’端编码区dna序列构建的树形图相同,表明完全可以用epsps基因3 ’端编码区dna序列代替基因全长编码序列作进化分析。
  • Hla - g1 , which is a newly defined non - classical hla class i molecule , plays an important role in mediating immunotolerance and protecting embryo and even some kinds of tumors from nk cells attacking . the full - length coding sequences containing cdna of hla - g1 were cloned from placenta , monocytes and liver cancer tissue of chinese donors . sequence analysis reveals that it is a highly conserved human gene with only two amino acid mutation sites compared to foreign nationality . its truncated form was overexpressed in
    从中国人外周血单个核细胞胎盘组织和肝癌组织等样品中克隆了包含完整hla - g1读框的cdna与国外同行获得的该基因及其蛋白质序列比较分析表明,该基因虽然有着细微的种族特异性,但高度保守并获得了它的截断型重组蛋白,根据蛋白一级结构和同源比较方法,模建了它及其与特异性受体kir2dl4形成复合体的空间结构模拟,预测了它们之间相互作用的特征。
  • The coding sequence of the two full - length cdnas were cloned by pcr , and inserted into expression vector pmet a between the downstream of a secreting signal peptide and the upstream of 6x histidine in the same reading frame with the coding sequence . the secreting recombinant expression vectors pmet a b / abp2304 and pmet a a / abp780 were constructed and transformed into pmad16 with lici transformation
    利用pcr技术将上述两个全长cdna的编码区克隆到表达载体pmet上,使之位于因子信号肽序列的下游, 6个组氨酸残基序列的上游,且与之同框,分别构建成融合蛋白分泌表达载体pmet b abp2304和pmet a abp780 。
  • We obtained the full length gene of hbfgf coding sequence with pcr , and adjusted the g + c content according the software dnasisv2 . 5 , and replaced the cys78 and cys96 with serines by site - directed mutagenesis . 2 . sequence result suggested one of the recombinant is correctly synthezied and cloned
    用pcr方法合成了hbfgf编码区全长,其中前20个氨基酸的g + c含量按暨南大学硕士学位论文:大肠杆菌表达重组hbfgf结构和功能优化摘要照计算机软件计算的结果进行了调整,第78和96位上的半眯氨酸被突变为丝氨酸。
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