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sequencing相关的网络例句

查询词典 sequencing

与 sequencing 相关的网络例句 [注:此内容来源于网络,仅供参考]

As part of an international effort to completely sequence the rice genome, we have produced a fine bacterial artificial chromosome-based physical map of the Oryza sativa japonica Nipponbare chromosome 4 through an integration of 114 sequenced BAC clones from a taxonomically related subspecies O.

国际水稻基因组测序计划(International Rice Genome Sequencing Project)采用以物理图为基础的随机测序战略,作为该计划的一部分,中国科学院国家基因中心承担了水稻第四号染色体精确序列的测定任务。

The termini of PCR products and the misincorporation in routine PCR were studied by using UT-PCR, cloning and sequencing.

应用UT-PCR扩增、克隆等对PCR产物末端研究结果表明,PCR产物末端组成是复杂多样的,但主要是3'端突出一个A,占末端总数的67.3%;其次是平端,占末端总数的26.9%。

The efficiency of selection was monitored by comparing the number of phage recovered from the acid elution and cell lysate in each round,and by testing EGFR binding specificity of polyclonal phagescFv on CHOEGFRGFP1 and CHOK1 cell with cell ELISA. Bacterial PCR was used to select clones containing a 1 kb insert. Cell ELISA was used to determine EGFR binding specificity of monoclonal pscFv on EGFR positive and negative cell. The number of individual EGFRbinding clones was determined with nucleotide sequencing. Results 500fold enrichments were observed by tittering phages in the cell lysate after five rounds of selection.

以稳定转染的CHOEGFRGFP1细胞和未转染的CHOK1细胞分别作为EGFR阳性和阴性细胞,采用负筛选的方法进行筛选;通过比较每轮投入及洗脱出噬菌体的效价比以及细胞ELISA检测多克隆pscFv与阳性、阴性细胞结合情况对筛选过程进行监测;采用菌落PCR挑选含有全长scFv片断的菌落,进一步用细胞ELISA检测单克隆pscFv与EGFR阳性及阴性细胞结合特异性;挑选EGFR特异性单克隆pscFv采用DNA测序法确定克隆多样性。

Results 500fold enrichments were observed by tittering phages in the cell lysate after five rounds of selection. A signal significantly greater than background binding was observed from the third to the fifth round of selection on CHOEGFRGFP1 and CHOK1 cell, but a part of polyclonal scFv bound EGFR specially. About 45% of the selected clones contained a fullsized insert of 1 kb. One unique human antiEGFR scFv (F4scFv) was isolated by analyzing with cell ELISA and DNA sequencing.

结果 经过5轮筛选,细胞裂解液中洗脱出噬菌体效价有500倍以上增长;细胞ELISA结果显示多克隆pscFv与CHOEGFRGFP1细胞和CHOK1细胞均有明显结合,但有部分特异性结合EGFR;菌落PCR显示约45%克隆中含有完整的1kb scFv片断;经细胞ELISA、 DNA测序检测共获得1株EGFR特异性单链抗体,命名为F4scFv。

Cell ELISA was used to determine EGFR binding specificity of monoclonal pscFv on EGFR positive and negative cell. The number of individual EGFRbinding clones was determined with nucleotide sequencing. Results 500fold enrichments were observed by tittering phages in the cell lysate after five rounds of selection.

以稳定转染的CHOEGFRGFP1细胞和未转染的CHOK1细胞分别作为EGFR阳性和阴性细胞,采用负筛选的方法进行筛选;通过比较每轮投入及洗脱出噬菌体的效价比以及细胞ELISA检测多克隆pscFv与阳性、阴性细胞结合情况对筛选过程进行监测;采用菌落PCR挑选含有全长scFv片断的菌落,进一步用细胞ELISA检测单克隆pscFv与EGFR阳性及阴性细胞结合特异性;挑选EGFR特异性单克隆pscFv采用DNA测序法确定克隆多样性。

Fifty-nine insect species have been included in genome sequencing projects, whole-genome sequences of six insect species, i.e., Drosophila melanogaster, Anopheles gambiae, Bombyx mori, Apis mellifera, Aedes aegypti and Tribolium castaneum, have been reported.

目前有59种昆虫已经列入基因组测序计划,其中6种昆虫(黑腹果蝇Drosophila melanogaster、冈比亚按蚊Anopheles gambiae、家蚕Bombyx mori、意大利蜜蜂Apis mellifera、埃及伊蚊Aedes aegypti和赤拟谷盗Tribolium castaneum)的全基因组序列已经报道。

One positive clone was obtained from the libraries with the tributyrin flat and ELISA sieve method. Analyzed the sequencing result, the positive clone include the Open Read Frame of low-temperature alkaline lipase gene.

序列测定分析表明,此重组质粒包含有长度为此95lbp的低温脂肪酶基因的完整的开放读码框架和上游调控序列。

Results The mecA gene and tst gene were detected,and were made the gene sequencing successfully.

结果 成功的对金黄葡萄球菌mecA基因和tst基因进行了检测,并进行基因测序。

The best bets for ultrarapid, low-cost sequencing are single-molecule approaches.

对于超高速、低花费的测序最好的办法是单分子的方式。

The effect of excess sludge reduction by uncoupler of 2,4-dechlorophenol was studied using Sequencing Batch Reactor.

采用序批式活性污泥反应器试验研究了解偶联剂2,4-二氯酚的污泥减量化效果。

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