1、

Sequence analysis of SSU rDNA variable region of different Leishmania isolates of China

利什曼原虫中国分离株ssu rDNA多变区序列分析

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2、

Aim To analyze the sequence of the SSU rDNA variable region of Leishmania isolates from desert and hill foci of China.

目的分析我国荒漠、山丘疫区利什曼原虫分离株的ssu rDNA多变区序列差异。

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3、

Three Gram-negative bacteria from commercial fresh fish were identified as Pseudomonas sp., an important food spoilage bacteria, on the basis of 16S rDNA sequences.

从市售鲜鱼中分离的3株革兰氏阴性菌,经16S rdna鉴定为假单胞菌属,该菌是一种导致食品腐败的重要腐败细菌。

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4、

Methods RAPD analysis and 5S rDNA spacer sequence were adopted.

方法随机扩增多态性DNA(RAPD)分析和5S rdna间隔序列差异。

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5、

Systematic Analysis of Complete Sequence of 16S rDNA of Bacillus in the Fermented Grain

酒醅中芽孢杆属细菌的16S rdna全序列系统学分析

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6、

identification of gastric and oral helicobacter pylori by pyrosequencing of the 16s rdna variable v1 regions

Pyrosequencing检测口腔与胃中的幽门螺杆菌16S rDNA V1区基因序列

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7、

in allium cepa, by using conventional electron microscopy and electron microscopy autoradiography, we investigated the morphological change of the nucleolar structure and the problem of rdna replication in the cell cycle.

本文以洋葱为材料,通过常规电子显微镜和电子显微镜放射自显影的方法,对核仁结构在细胞周期中的变化规律和rDNA的复制问题进行了研究。

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8、

simple amplification of gc-rich repetitive sequences in bos taurus rdna with pcr

通过PCR技术简单扩增奶牛高GC含量的rDNA重复序列

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9、

The D 1-D 2 region of LSU ( large subunit ) rDNA and total ITS 1-5.8 S-ITS 2 were amplified, cloned and sequenced.

本株纤小裸甲藻大亚基D1~D2区序列长度为721bp, 与基因库中该种的一株相似种同源性超过99%.

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10、

These yam germplasms exhibited extensive genetic variability, there were plent of utilize space in breed-cultivated process. 16S rDNA PCR-RFLP cluster analysis and REP-PCR cluster analysis indicated that there is a great genotypic diversity of Pseudomonas fluorescens.

由此可见,我国山药品种资源具有丰富的遗传多样性,在品种选育亲本选择上有很大的利用空间。16s rDNA PCR-RFLP和REP-PCR分析揭示了荧光假单胞菌存在高度的遗传多样性。

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11、

Rapid Detection of Pseudomonas aeruginosa by the Fluorescence Quantitative PCR Assay Targetting 16S rDNA

16S rdna用作荧光定量PCR靶基因快速检测铜绿假单胞菌

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12、

Analysis of 5S rDNA and Centromeric Sequences in Rice by Fiber-FISH

水稻5S rdna和着丝粒顺序的Fiber-FISH分析

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13、

Cloning and SNP Analysis of rDNA-ITS 2 of Anopheles anthropophagus

嗜人按蚊rDNA-ITS2基因的克隆鉴定及SNP分析

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14、

Phylogenetic Relationships of the Main Bryozoan Lineages Based on LSU ( 28S) rDNA Sequences

基于LSU(28S)rDNA证据探讨苔藓动物主要分类群的系统演化关系

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15、

Isolation and 16S rDNA sequence analysis of extremely halophilic archaea from Saline in Altun region

阿尔金山盐湖极端嗜盐古生菌的分离及16S rdna序列分析

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16、

28s rDNA molecular morphology of the main bryozoan lineages and its phylogenetic significance

苔藓动物主要类群28S rdna多变区的分子形态分析及其系统学意义

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17、

The main results were as follows: 1. We further confirmed the genus and species name of strain 34-9 by using rDNA-ITS molecular identification.

主要研究结果如下:1.利用rDNA-ITS分子鉴定,进一步证实了菌株34-9的属、种名。

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18、

Meanwhile, the citrus chromosome slides used for FISH and rDNA loci situation on chromosome, genetic variation analysis among the homologous tetraploids and diploids, repeated sequence of chromosome in situ hybridization ( CISH) for chromosome identification and species evolvement were discussed.

对用于荧光原位杂交的柑橘染色体制片方法和rDNA在染色体上的分布位置、同源四倍体和相应二倍体的遗传差异分析、重复序列的染色体原位杂交用于染色体识别和物种演化研究等进行了讨论。

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19、

In the late-G1 phase, rDNA replication began.

rDNA的复制时期最早起始于G1期的较晚时期,此时只有少数细胞核仁中的rDNA进行复制;

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20、

Analysis on Molecular Systematics of Chironomus rDNA in Water Treatment Plants

自来水厂中摇蚊rDNA系统学分析

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