编码序列

cDNA捕捉法&从大的基因组区域直接分离编码序列

CDNA capturation ─ Isolation of coding sequences from large genomic region

人们已经从数十种脊椎动物和无脊椎动物中克隆了AChE的编码序列。

AChE coding sequences have been cloned so far from a range of evolutionarily diverse vertebrate and invertebrate species .

DNA编码序列的关联特性

A Critical Review on the Correlation Properties of Coding DNA Sequences

选择了4个信息参数来描述核酸序列的序列特性，以线虫染色体上顺次排列的DNA序列、基因间序列和编码序列片段为序列单元，分析各个单元的序列特性沿着染色体排列的顺序关系。

Four information parameters are selected to depict the characteristic of nucleotide sequences .

DNA编码序列的图形表示及相似度计算

Graphical Representation and the Similarity of DNA Primary Sequences

重叠延伸PCR法在合成人骨保护素N端编码序列中的应用

Amplification of DNA sequence Encoding N-terminal Fragment of Osteoprotegerin Using Overlap-extension PCR

DNA计算中，需要将实际问题映射成DNA编码序列，这就是DNA编码。

In DNA computing , DNA encoding is a module that the practical problems are mapped to the DNA sequence .

从人T细胞淋巴瘤cDNA文库中筛选含PH结构域编码序列的新基因

Screening new genes containing PH domain coding sequence from human T cell lymphoma cDNA library

氨基酸序列分析表明，其N端第17～25位氨基酸序列与Tropic1808基因编码序列一致。

Amino acid sequence analysis showed that 17 to 25 amino acid sequences of N terminus were consistent with Tropic 1808 gene .

小鼠金属硫蛋白ⅠcDNA编码序列的克隆及其在昆虫细胞中的表达

The Clone of Mouse Metallothionein ⅰ cDNA Coding Sequence and Its Expression in Insect Cells

用PCR扩增法合成鼠IgG轻链隹号肽的编码序列。

The Sequence encoding the Signal Peptide of Kappa Chain of Mouse IgG was synthesized by PCR amplification .

以含有抗生链霉菌酪蛋白酶基因的质粒pIJ702为模板，用PCR方法扩增得到了melC1的信号肽编码序列及其上游的调控序列。

The melC 1 signal peptide-encoding sequence and its upstream sequence originated from S. antibioticus was also amplified by PCR technique .

通过cDNA测序分析剪切位点突变引起编码序列的变化。

The cDNA sequencing was performed to analyze the change of FV coding sequence by splice site mutation .

然而DNA编码序列的设计需要同时考虑物理化学属性以及热动力学特性等约束条件，传统的优化方法很难对其进行求解。

DNA sequence design need meet simultaneously several physical , chemical and logical constraints , which is difficult to be solved by the traditional optimization methods .

结果：bax基因编码序列及嵌合基因限制性酶谱正确；

Results : The coding sequence of bax and pSV-CIP-bax-CAT gene was characterized by restriction analysis .

目的构建携带淋球菌主要外膜蛋白PIA基因的pET重组质粒，分析其编码序列。

Objective To construct a recombinant plasmid harbouring the PIA gene of Neisseria gonorrhoeae .

目的：克隆小鼠载脂蛋白CⅡ（ApoCⅡ）编码序列。

Objective : To clone the DNA fragment encoding mouse apolipoprotein C ⅱ( ApoC ⅱ) .

方法本文根据G蛋白多肽碱基序列的需要，设计并合成了带有突变核苷酸序列的寡聚核苷酸引物，以G基因RT-PCR产物为模板，采用高保真DNA聚合酶，PCR突变扩增，得到G蛋白多肽编码序列。

Methods : Based on the base sequence of the G-protein polypeptide , the oligonucleotide primers were designed and synthesized which contains the mutational nucleotide sequence .

结果成功克隆了Canstatin基因cDNA编码序列并获得测序证实。

Result The canstatin cDNA coding sequence was successfully cloned and sequenced .

22株猪瘟病毒E2基因部分编码序列的序列分析

Sequence analysis of the partical coding sequence of E2 gene of 22 hog cholera virus strains

核基质附着区（matrixattachmentregions，MARs）是与核基质（或核骨架）特异结合的DNA序列，属于非编码序列，富含AT。

Matrix attachment regions ( MARs ) are DNA sequences that bind to the nuclear matrix , which tend to be noncoding sequences and AT rich .

本文采用膜优化算法优化DNA计算编码序列，提出了一类求解DNA编码问题的新方法，扩展了膜计算的应用领域。

In this dissertation , Membrane optimization algorithm is applied in finding sequences suitable for reliable DNA computing in this thesis , a new method of DNA sequence design is pu .

对120个较短编码序列（<1200bp）的Fourier频谱进行分析表明，3碱基周期性在短编码序列中并不是绝对存在的。

Fourier spectra of 120 short coding sequences ( < 1 200 bp ) show that not all coding sequences are characterized by 3 base periodicity .

经过拼接，获得了全长的ob基因编码序列。

The full length coding region of ob gene was obtained by in vitro splicing with ligase .

鹌鹑gcl基因BTB/POZ结构域编码序列的克隆及组织中的表达

Cloning and Expression of Quail gcl BTB / POZ Domain Coding Sequence

利用PCR反应得到了26个水稻蛋白激酶的编码序列；为了提高同源重组的效率，降低引物合成的成本，试验采用两次PCR方法使重组位点达到50bp，明显提高了转化效率；

And 26 encoding sequences of these kinases were obtained through two rounds of PCR , enhancing the efficiency of transformation ;

最后，将Costas频率编码序列和Pushing频率编码序列相结合，提出一种将上述两种序列信号联合用于目标探测的方案。

Finally , we propose a scheme which combines the Costas frequency coded sequences and Pushing frequency coded sequences for target detection .

结果1、合成人CD28分子的基因序列，经DNA序列分析证实合成的基因序列为人CD28编码序列。

Synthesis the sequence of gene of CD28 molecules , and it confirmed to be coding sequence of CD28 by DNA sequence analysis . 2 .

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 .

对重组质粒的分析表明，插入片段的序列与发表的VDR基因编码序列相同。

The sequence of the insert in the plasmid was identical to the published coding-region sequence of VDR gene .