1)16S rDNA16SrDNA
1.Bacterial diversity study for the simultaneous nitrogen and phosphorus removal system (MDAT-IAT) by 16S rDNA cloning method;16SrDNA克隆文库方法分析MDAT-IAT同步脱氮除磷系统细菌多样性研究
2.Community of Activated Sludge Based on Different Targeted Sequence of 16S rDNA by Denaturing Gradient Gel Electrophoresis;不同16SrDNA靶序列对DGGE分析活性污泥群落的影响
3.Identification of Sarcosaphagous Flies by Analyses the Sequence of 16S rDNA;16SrDNA序列分析在嗜尸性蝇类鉴定中的应用
英文短句/例句
1.The Sequence Analysis of 16S rDNA of Ralstonia solanacearum from Guangdong广东茄科雷尔氏菌16SrDNA序列分析
2.Application of 16s rDNA-Sequential Analysis in Classification and Determination of Micro-Organism;16SrDNA序列分析技术在微生物分类鉴定中的应用
3.Identification of Sarcosaphagous Flies by Analyses the Sequence of 16S rDNA;16SrDNA序列分析在嗜尸性蝇类鉴定中的应用
4.Optimal Amplifying Conditions of Soil Microbial 16SrDNA From Desert Steppe荒漠草原土壤微生物16SrDNA扩增反应条件的优化
5.Oligonucleotide Microarray for Identification of Bacteria Basing on the 16SrDNA Gene s Polymorphism;基于16SrDNA多态性的细菌鉴定寡核苷酸芯片的初步研究
6.Preliminary Study on Morphology of Ossicles, Biochemical Components and mt16S rDNA Sequences of 15 Sea Cucumbers;15种海参骨片形态、生化组分及线粒体16SrDNA序列的初步分析
7.Cultural Condition, Colonizing Dynamics and 16SrDNA Sequence Analysis of PGPR Strains Isolated from Gramineous Forage;禾本科牧草根际促生菌适宜培养条件和定殖动态研究及其16SrDNA序列分析
8.Molecular Phylogenetics of Rhinolophus (Chiroptera: Rhinolophidae) in Guizhou Based on Mitochondrial 16S rRNA Gene基于线粒体16SrDNA的贵州菊头蝠属（翼手目：菊头蝠科）的分子系统进化关系
相关短句/例句
16S rDNA-DGGE16SrDNA-DGGE
3)16S rDNA PCR16SrDNA PCR
4)16S rDNA-PCR16SrDNA-PCR
5)16S rDNA sequence16SrDNA序列
1.In order to know the compositions and changes of pronucleus microbial floras in the fermented grains in the pits for Luzhou-flavor liquor, the techniques including PCR technique and 16S rDNA sequence homology analysis etc.为了探讨中国传统白酒窖池糟醅中的原核微生物区系的构成及变化,运用PCR扩增技术和16SrDNA序列同源性分析等方法测定糟醅中原核微生物的16SrDNA基因全序列,根据与基因数据库中相似菌群16SrDNA序列的同源性,分析窖池糟醅中原核微生物的生理特性和区系分布。
2.【Method】 The scab-related strains were analyzed according to the biological characteristics and the 16S rDNA sequences.【方法】采用结合生物学特性和16SrDNA序列特点的方法对获得的菌株进行分析。
3.Homology analysis showed that its 16S rDNA sequence has the identity of 100% compared to Streptomyces microflavus.对这株具有高效溶藻效果能力的放线菌AN02分别进行了形态特征、培养特征及生理生化特性的分析,分析结果表明放线菌AN02菌株的上述几个特征与细黄链霉菌(Streptomyces microflavus)的高度一致,与此同时,聚类分析结果也同样表明,放线菌AN02菌株与细黄链霉菌(Streptomyces microflavus)的高度一致,后经过比对,发现二者的16SrDNA序列的同源性高达近100%,因此,可将溶藻放线菌AN02定名为细黄链霉菌AN02(Streptomyces microflavus AN02)。
6)16S rDNA sequencing16SrDNA测序
1.Methods Phenotypic characteristics,chemotaxonomic analysis,16S rDNA sequencing were applied.方法 用表型性状、化学分类和 16SrDNA测序鉴定并作药敏试验。
延伸阅读
(16-alpha,17-beta)-estra-1,3,5(10)-triene-3,16,17-triolCAS：50-27-1分子式：C18H24O3分子质量：288.38熔点：281-282℃中文名称：雌三醇；16,17-二羟甾醇英文名称：(16-alpha,17-beta)-estra-1,3,5(10)-triene-3,16,17-triol (16-alpha,17-beta)-oestra-1,3,5(10)-triene-3,16,17-triol 1,3,5-estratriene-3-beta,16-alpha,17-beta-triol 1,3,5-oestratriene-3-beta,16-alpha,17-beta-triol 16-alpha,17-beta-estriol 16-alpha,17-beta-oestriol用途：治疗白细胞减少症，对前列腺肥大、前列腺癌也有一定疗效。
