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1)  16S rRNA sequence
16S rRNA序列
1.
Method: Based on Physiological and biochemical experiments and the analysis of 16S rRNA sequence.
方法:基于生理生化实验和16S rRNA序列分析。
2)  16S rRNA gene sequence
16S rRNA基因序列
1.
The significative 2 strains were classified according toculture characteristics, modality characteristics, characteristic reaction, and comparing16S rRNA gene sequence with other 5 strians.
通过与其他5株活性菌株的16S rRNA基因序列比较,并结合生理生化、形态特征和培养特征分析,探讨了这两株菌的分类地位。
2.
The 16S rRNA gene sequence of the two isolates were amplified and compared with those of other Streptococcus retrieved from GenBank.
对2个分离株的16S rRNA基因进行PCR扩增和测序,并与GenBank中收录的链球菌16S rRNA基因进行序列分析并构建系统进化树,结果显示,2个分离株的16S rRNA基因序列相同,与停乳链球菌同源性最高达97。
3)  16S rRNA~23S rRNA Intergenic spacer regions
16S rRNA~23S rRNA间断序列
4)  sequences analysis of 16S rRNA gene
16S rRNA基因序列分析
5)  16S-23S rRNA intergenic spacer sequence
16S-23S rRNA间隔区序列
6)  16S rDNA sequence
16S rDNA序列
1.
Based onphenotypic characteristics and 16S rDNA sequence analysis, ten isolates were identified as Pseudomonasspp.
根据其生理生化性状和 16S rDNA序列分析结果表明,分离菌株 EVA5,EVA6,EVA7,EVA8和 EVA9为假单胞菌(Pseudomonas spp。
2.
The 16S rDNA sequence homology between the strain 24# and model strain S.
16S rDNA序列分析显示本菌株与模式菌株链霉菌DSM44293T的16SrDNA同源性为98。
3.
Further studies on 16S rDNA sequences,physiological and biochemical test of 8 different strains showed that 16S rDNA PCR-RFLP analysis is rapid and easy way to identify large scale of Lactobacillus.
根据16S rDNA-RFLP的结果从中选出8株有代表性的菌株进行生理生化实验和16S rDNA序列的测定,实验结果与RFLP鉴定结果相吻合,表明此方法是一种快速、准确的可用于大量乳杆菌分类和鉴定的方法。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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