助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   sequence analysis results 的翻译结果: 查询用时:0.192秒
图标索引 在分类学科中查询
所有学科
生物学
更多类别查询

图标索引 历史查询
 

sequence analysis results
相关语句
  序列分析结果
     Sequence analysis results indicated that the homology of complete genome nucleotide sequence from strain NA-1 was between 81.2% and 91.3% as compared withrepresentative strains from every locals.
     序列分析结果表明,GPMVNA-1株与各地代表株核苷酸同源性81.2%~91.3%。
短句来源
     Sequence analysis results consistently provide new taxonomy evidence at the DNA level for supporting Ratajszczak and Groves’ viewpoint that N. intermedus is merely the adult of N. pygmaeus (Ratajszczak,1998;Groves,1971).
     在DNA水平上 ,序列分析结果一致地提供了新的分类学证据 :支持Rata jszczak和Groves的观点 ,即N intermedus只是N pygmaeus的成体 (Ratajszczak ,1998;Groves ,1971)。
短句来源
     Sequence analysis results showed that RBSDV S9 (1 900 bp) contained two non-overlapping ORFs encoding 39.9 ku and 24.2 ku proteins respectively. The sequence homology was 89% between Chinese RBSDV S9 and Japanese RBSDV S9 and 86% between Chinese RBSDV S9 and Italian MRDV S8.
     序列分析结果表明 :S9全长 190 0bp ,含有 2个不重叠的ORF ,编码蛋白的分子质量分别为 39.9,2 4.2ku ,与日本株S9核苷酸序列同源性为 89%,与意大利株MRDVS8同源性为 86 %.
短句来源
     2.Construct the eukaryotic expressing vector of hEGF and analyse the sequence of hEGFhEGF gene was transfered from PGEM-TEasy- hEGF into eukaryotic expressing vector-pcDNA3.1. The sequence analysis results show that base pair homology is 98.2% between hEGF gene and Genebank sequence.
     2.hEGF基因真核表达载体构建及序列分析经Hindlll、Ba栩I酶切PGEM一TEasy一hEGF,将hEGF基因定向克隆到真核表达载体pcDNA3.1中。 序列分析结果表明,pcDNA3.1一hEGF基因序列与Genbank hEGF序列相比,二者碱基同源性达98.2%,为相同的氨基酸编码。
短句来源
     The FP1 gene was amplified from pGEM-FP1 vector by polymerase chain reaction (PCR) and inserted into the pUCM-T vector constructed to pUCM-FP1. The DNA sequence analysis results showed that the amplified target fragment was correct completely.
     通过PCR 反应从pGEM-FP1载体上扩增FP1基因,并插入pUCM-T 载体构建成pUCM-FP1中间载体。 PCR和酶切鉴定正确的克隆进行测序,序列分析结果表明,插入目标序列完全正确。
短句来源
更多       
  “sequence analysis results”译为未确定词的双语例句
     The sequence analysis results showed that the sizes of PB2、PB1、PA、HA、NP、NA、M and NS gene were respectively 2341 bp, 2341bp, 2233bp, 1779bp, 1565bp, 1398bp, 1027bp and 890bp.
     测序结果表明:PB2、PB1、PA、HA、NP、NA、M和NS基因的大小依次为2341bp、2341bp、2233bp、1779bp、1565bp、1398bp、1027bp和890bp。
短句来源
     Amino sequence analysis results indicate the 3 peptides containing 2 conserved motifs: SNPIHII and NIP.
     经过多肽序列分析发现这3个十五肽具有2个保守序列,分别是第2至8个氨基酸残基SNPIHII和第12~15个氨基酸残基NIP。
短句来源
     Sequence analysis results showed that CYP6B29 contains a(1 518 bp) open reading frame,which encodes 505 amino acid residues(m.w.58 kD,pI 8.29).
     序列分析表明,该基因的ORF为1 518 bp,编码505个氨基酸,预测其相对分子质量约为58 kD,等电点为8.29。
短句来源
     Sequence analysis results showed that clone HN-K had 98% nucleotide sequence identity with Portuguese isolate 28C and Israeli stem pitting isolate VT;
     序列分析表明,克隆HN-K与葡萄牙分离物28C和以色列茎陷分离物VT的同源性均为98%;
短句来源
     Sequence analysis results showed that iap1 of BmNPV-ZJ contains 858 base pairs of nucleotides, with 96% identity in nucleotides, but missing a region which encodes seven continuous aspartic acids, compared to that of BmNPV-T3 strain.
     序列同源分析表明 :BmNPV ZJ的iap 1全长为 85 8bp ,与BmNPV T3株的碱基同源性为 96 % ,与BmNPV T3株相比少了一段编码 7个氨基酸的区域 ,该缺失区域的两侧有着独特的结构 :缺失区的 5′侧为连续编码 7个天冬氨酸的序列 ; 缺失区的 3′侧为连续编码3个天冬氨酸的序列。
短句来源
更多       
  相似匹配句对
     Sequence analysis showed that the E.
     序列测定和计算机联配结果表明:E.coli FGA与Genebank AF237653一致;
短句来源
     On Electric Sequence Analysis
     电序分析
短句来源
     sequence.
     序列的情形作了相应的推广
短句来源
     (N, W) Analysis
     关于点系结构的分析
短句来源
     analysis.
     分析表明,其单糖组成为Glc。
短句来源
查询“sequence analysis results”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  sequence analysis results
Sequence analysis results are displayed to the right of the corresponding IHC image.
      
Red boxes indicate examples of pair that are 13 supported by comparative sequence analysis results shown in D.
      


Objective To develop a sensitive and specific reverse nested polymerase chain reaction(RT nested PCR)method for the detection of hepatitis G virus (HGV) in Chinese patients. Methods A set of nested PCR primers were designed according to the sequence analysis result of partial NS5 gene of HGV in Chinese patients. Using this set of primers, a RT nested PCR method was developed to detect HGV infection in the Chinese, and its result was compared with one stage PCR and nested PCR, whose primers...

Objective To develop a sensitive and specific reverse nested polymerase chain reaction(RT nested PCR)method for the detection of hepatitis G virus (HGV) in Chinese patients. Methods A set of nested PCR primers were designed according to the sequence analysis result of partial NS5 gene of HGV in Chinese patients. Using this set of primers, a RT nested PCR method was developed to detect HGV infection in the Chinese, and its result was compared with one stage PCR and nested PCR, whose primers were designed according to sequences from abroad. Results 133 samples were detected. The positive rate in one stage PCR, nested PCR and our newly developed nested PCR was 8.3%, 11.3% and 18.0% respectively. The specificity of the PCR product was verified by sequence analysis. Conclusion Our developed RT nested PCR method markedly increased the positive rate of HGV RNA among Chinese patients.

目的建立敏感、特异的逆转录套式聚合酶链反应(RT-nested-PCR)方法,以检测中国人庚型肝炎病毒(HGV)感染。方法根据中国人感染HGV者NS5区部分核苷酸序列分析结果,设计套式PCR引物,用于HGVRNA的检测,并与用国外报道引物所作的一次PCR和套式PCR检测结果进行比较。结果共检测标本133份。以国外报道引物作一次PCR和套式PCR检出率分别为8.3%和11.3%,作者建立的套式PCR检出率为18.0%,对部分PCR产物进行序列分析证实为HGV特异性基因。结论建立的方法可在中国人群中显著提高HGVRNA检出率。

The soluble hydrogenase from C.vinosum was consist of two subunits (52 kDa, 21.5 kDa). According to the N terminal sequences of the large subunit: N’ SRTITIEPVTRXEGHAR and the small subunit: N’ STQPKITVATXLDG, Primer 1: 5’ gAT (g/C)gT gAT (g/C)gT (g/A)Cg 3’ and Primer 2: 5’ A gC AC(C/g) CAg CC(C/g) AA(g/A) ATC 3’ were synthesized and applied for PCR to amplify the fragment encoding the small subunit. The sequence analysis results showed that the soluble hydrogenase contained the reserved motif: CxxC......GxCxxxG......GCPP,...

The soluble hydrogenase from C.vinosum was consist of two subunits (52 kDa, 21.5 kDa). According to the N terminal sequences of the large subunit: N’ SRTITIEPVTRXEGHAR and the small subunit: N’ STQPKITVATXLDG, Primer 1: 5’ gAT (g/C)gT gAT (g/C)gT (g/A)Cg 3’ and Primer 2: 5’ A gC AC(C/g) CAg CC(C/g) AA(g/A) ATC 3’ were synthesized and applied for PCR to amplify the fragment encoding the small subunit. The sequence analysis results showed that the soluble hydrogenase contained the reserved motif: CxxC......GxCxxxG......GCPP, which existed in all NiFe hydrogenases. C.vinosum soluble hydrogenase is a new NiFe hydrogenase which contained only one [4Fe 4S].

光合细菌 C.vinosum可溶性氢酶由 52 k Da和 2 1.5k Da两个亚基组成 .该酶大亚基 N-末端氨基酸序列为 :SRTITIEPVTRXEGHAR,小亚基 N末端氨基酸序列为 :STQPKITVATXL DG.根椐大、小亚基 N-末端氨基酸序列设计两套引物 ,Primer1:5′g AT(g/ C) g T g AT(g/ C) g T(g/ A) Cg3′和 Primer2 :5′A g C AC(C/ g) CAg CC(C/ g) AA(g/ A) ATC3′,通过 PCR扩增获得 0 .6 kb的扩增片段 .克隆并对该片段序列进行分析 ,结果表明 ,该片段包含小亚基基因的全序列 .可溶性氢酶小亚基由 179个氨基酸残基组成 ,分子量为 2 1.8k Da,含有 Ni Fe-氢酶保守的序列框 :Cxx C......Gx Cxxx G......GCPP

The biological properties of Shenyang isolated strain(designated as SY) of avian infectious bronchitis virus(IBV) were character- ized, and the nucleotide sequences of major immunogenetic S1 genes were cloned,determined and compared with the published S1 gene sequences. The isolated strain SY was identified as an IBV by morphological characterization , embryoed chicken eggs inoculation and hemagglutination essay. Virus neutralization with chicken tracheal organ cultures(TDCs) showed that the isolated...

The biological properties of Shenyang isolated strain(designated as SY) of avian infectious bronchitis virus(IBV) were character- ized, and the nucleotide sequences of major immunogenetic S1 genes were cloned,determined and compared with the published S1 gene sequences. The isolated strain SY was identified as an IBV by morphological characterization , embryoed chicken eggs inoculation and hemagglutination essay. Virus neutralization with chicken tracheal organ cultures(TDCs) showed that the isolated SY was a new variant of IBV that was either different from the standard reference strains such as T,H52 and M41 strains or different from the othar strains HD,HB,XB and DB isolated in china. Based on the published IBV genomic sequences,a pair of specific primers was designed and synthesized for amplification of the S1 genes of the isolates SY. A DNA fragment predicted size of approximately -1 .7kb was amplified by reverse transcription and polymerase chain reaction (RT-PCR) using the purified viral RNA as template.The PCR products were digested with Bam HI and Eco R2 and then ligated with the plas- mid pUC19 cut with the same restriction endonucleases.The white colonies carrying recombinant plasmids were selected from LB agar plates. The positive recombinants were identified by restriction endonuclease digestion and PCR amplification. The nucleotide sequence of whole S1 gene of 1640 bp was determined with ABI PRISM 377 DNA Sequencer. Phylogenetic analysis of the S1 gene nucleotides and predicted amino acids revealed that the isolates SY had less than 80% similarity with the standard reference strains and domestic dominant strains.The serum antibody neutralization test and nucleotide sequence analysis results demonstrated that the isolate SY was a new variant IBV in China.

本研究对分离自沈阳地区的一株传染性支气管炎病毒(SY毒株)进行了生物学特性的研究,同时成功地对其免疫原S1基因进行了RT-PCR扩增、克隆与序列分析。 通过电镜观察、动物回归试验、血凝特性研究等试验验证分离自沈阳地区的SY毒株确实为一株传染性支气管炎病毒。气管环组织培养交叉中和试验结果表明,分离株SY株不同于参考毒株澳大利亚T、H52、M41,且不同于国内其它流行株HD、HB、XB、DB等,是一个新的变异株。 利用IBV S1基因特异性寡聚核苷酸引物,经RT-PCR扩增SY毒株的S1基因,得到预期的约1.7Kb片段;并将扩增所得cDNA插入克隆质粒pUC19的EcoRⅠ/BamHⅠ位点,在大肠杆菌DH5a中实现目的基因的克隆。经限制性核酸内切酶分析及PCR鉴定,证实为阳性重组质粒,利用末端双脱氧链终止法对其测序,得到S1基因全长1640bp,包括整个开放阅读框。通过序列分析软件DNASIS、PROSIS、MEGA等软件对S1基因核苷酸序列及推导的氨基酸序列进行分析,结果表明:分离株SY与7株参考株和国内流行株HD株相比,无论是核苷酸序列同源百分率还是氨基酸序列同源百分离都较低,均未达到80%,这就提示我们SY毒

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关sequence analysis results的内容
在知识搜索中查有关sequence analysis results的内容
在数字搜索中查有关sequence analysis results的内容
在概念知识元中查有关sequence analysis results的内容
在学术趋势中查有关sequence analysis results的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社