阅读框架

  • 网络Reading frame;ORF;ORFs;open reading frame, ORF
阅读框架阅读框架
  1. DNA芯片分析HBV阅读框架多点基因突变的研究

    Gene chip analysis of mutation of HBV-DNA open reading frame

  2. 其cDNA开放阅读框架编码1765个氨基酸。

    Its cDNA open reading frame encodes 1765 amino acids .

  3. DNA序列测定显示所得克隆的开放阅读框架长843bp。

    The detection of DNA sequence showed that the length of the obtained cloning open-reading frame was 843 bp .

  4. 以该文库DNA为模板,运用PCR方法扩增出360bp的NGF和616bp的CNTF阅读框架片段。

    The cDNA of NGF and CNTF was amplified by the method of PCR .

  5. 测序结果表明,该毒株的HA基因全长为1745bp,含有完整的阅读框架,编码566个氨基酸;

    The HA gene was 1 745 bp in length and coded for 566 amino acids .

  6. 经序列分析,此cDNA为一个567bp长的开放阅读框架,编码由188个氨基酸组成的病毒外壳蛋白。

    The cDNA was 567 bp in length with open reading frame of 188 amino acids .

  7. K562细胞未知基因KH的开放阅读框架在大肠杆菌中的表达

    The expression of open reading frame of unknown KH gene from K562 cells in E.coli

  8. 基因测序结果表明,该cDNA具有独立的开放阅读框架,编码1个由344个氨基酸残基构成的可溶性蛋白分子,属于免疫球蛋白超家族成员。

    DNA sequencing analysis showed that the cDNA had an open reading frame encoding 344 amino acid residues without transmembrane domain and belonged to immunoglobulin superfamily .

  9. 进一步DNA测序结果显示插入片段与tsbp编码序列一致,阅读框架完整,并且无移码。

    Further DNA sequencing manifested that the insertion element was tsbp sequence with complete reading frame and no frame shift .

  10. 未知基因KH开放阅读框架真核表达载体的构建及其对K562细胞增殖的影响

    Construction of eukaryotic expression vector of open reading frame of unknown KH gene and its effect on proliferation of K562 cell

  11. 其HN基因开放性阅读框架(ORF)为1716bp,编码571个氨基酸;

    Its HN gene has an opening reading fragment ( ORF ) of 1,716 bp and it encodes 571 amino acids .

  12. 测序结果表明所扩增的cDNA含有完整的开放阅读框架(ORF),有1410个核苷酸,编码470个氨基酸。在www。

    The sequence indicates that the cDNA amplified by RT-PCR has a complete Open Reading Frame ( ORF ) with 1410 nucleotide acids encoding 470 amino acids .

  13. 结果表明:2毒株HN基因开放性阅读框架(ORF)均为1716nt;

    The results showed that : strain YN-C1 and YN-C2 all have 1 716 nt opening reading fragment ( ORF ) length ;

  14. 方法通过基因芯片技术,将HBVdna进行PCR扩增,掺入荧光分子标记,与点阵列的寡核苷酸杂交,通过计算机分析,检测HBVdna的基因序列,观察HBVdna阅读框架各位点的自然变异。

    Methods By using gene chip technique , HBV-DNA was amplified by PCR , incorporated with fluorescence , hybridized with oligonucleotide to detect the gene sequence of DNA by computer analysis and observe the natural mutation of HBV-DNA ORF .

  15. 开放阅读框架(ORF)453bp,共编码150个氨基酸。

    Bp 3 ' - untranslated region and 453 ? bp open reading frame ( ORF ), which encodes 150 amino acids .

  16. 所有克隆到的gp120基因都具有完整的阅读框架,无大的缺失和插入。

    All the Cloned gp120 genes have the complete open reading frames , and no major deletion and insertion .

  17. 结合位置权重矩阵(PWM,positionweightmatrix)和开放阅读框架(ORF,Openreadingframe)的长度分布特征建立了简单的方法识别翻译起始位点,此方法能很好地区分上游AUG和TIS。

    Based on the position weight matrix ( PWM ) and length distribution of open reading frame ( ORF ), a simple method for predicting translation initiation sites is presented . It can identify TIS from upstream AUGs easily .

  18. 目的:构建K562细胞未知基因KH的开放阅读框架(openreadingflame,ORF)的原核表达体系。

    Objective : To construct the prokaryotic expression system of open reading frame of KH gene ( KH-ORF ), an unknown gene in K562 cells .

  19. 它在进化上具有高度保守性,是一组不编码蛋白质,不具有开放阅读框架(ORF)的短序列RNA。

    It is highly conserved in evolution , which is a set of encoded protein that does not have a short sequence of RNA open reading frame ( ORF ) .

  20. 提出了一个预测DNA序列中无内含子的开阅读框架(ORF)的理论方法&终止密码预测法;

    A method for predicting first kind of open reading frame ( ORF ) is given , which is called Terminal Codon Method . The first kind of ORFs is the ORF that has not intron in it .

  21. 目的构建未知基因KH的开放阅读框架(KHORF)的真核表达体系,初步探讨未知基因KH对细胞增殖的影响。

    Objective To construct an eukaryotic expression vector of open reading frame of unknown KH gene ( KH ORF ), and investigate its effect on cell proliferation .

  22. 比较2种阅读框架,以保守序列作为模板扩增得到完整的编码EIAV反式激活蛋白的基因。

    The whole sequence of tat gene has been obtained by further polymerase chain reaction during which more conservative sequence was used as template .

  23. 结果限制性核酸酶切及序列分析表明重组表达质粒包含Pokemon基因编码区,阅读框架无移位;

    Results Restriction enzyme digestion and DNA sequencing suggested that the recombinant expression plasmid contained correct encoding region of Pokemon , without reading frame shift .

  24. 序列分析的结果表明,此3.1kb外源片段中存在一长度为1347bp的完整的开放阅读框架(ORF),起始密码子为ATG,终止密码子为TGA,共编码448个氨基酸。

    Sequence analysis revealed that the open reading frame of mcr gene was 1 347 bp in size , encoding 448 amino acids with ATG as initiation codon and TGA as termination codon .

  25. 真核基因起始与终止密码子旁侧序列的特征对于确定cDNA开放阅读框架(ORF)和预测基因组序列中的编码区(CDS)非常重要。

    The characters of sequence flanking the start codon and stop codon in eukaryotic genes play an important role in defining the open reading frame ( ORF ) in cDNA sequences and coding region ( CDS ) in genomic DNA sequences .

  26. ERIC(IRU)局限于基因组可转录区,即多顺反子操纵子基因间区域,或开放阅读框架上、下游非翻译区。

    ERIC ( IRU ) is restricted to transcribed regions of the genome , either in intergenic regions of polycistronic operons or in untranslated regions upstream or downstream of open reading frames ( ORF ) .

  27. 小鹅瘟病毒GPV-YG株主要开放性阅读框架核苷酸序列分析

    Analysis of the Major Open Reading Frames ' Nucleotide Sequence of Goose Parvovirus GPV-YG Strain Isolated in China

  28. PTI基因翻译起点上游具有‘TATA’和‘CCAAT’等转录控制元件,其包含的最大阅读框架能编码一个213aa的多肽。

    The longest open reading frame in the PTI gene , which contains conventional ' TATA ' and ' CCAAT ' transcription control elements , potentially encode a peptide of 213 amino acids .

  29. 测序结果表明该680bp片段含一个开放阅读框架,编码204个氨基酸,其中N端17个氨基酸为信号肽,中间43个氨基酸为Hevein成熟肽,C端144氨基酸为未知功能多肽。

    The sequence analysis indicated that the fragment had a complete open reading frame that encoded a polypeptide of 204 amino acids with the N-terminal region containing 17 amino acids signal peptide , the mature hevein containing 43 amino acids and the C-terminal region containing 144 amino acids polypeptide .

  30. 利用载体pET-22b(+),构建chiB表达载体pET-chiB,通过验证分析表明,所克隆的基因chiB已置于表达载体的正确阅读框架下;

    Utilizing vector pET-22b ( + ) to construct expression vector pET - chiB , through validating and analyzing , the result indicated that the cloned chiB gene had been inserted the correct reading frame of expression vector ;