1) SSU rDNA sequences
小亚基rDNA序列
2) small subunit rDNA
rDNA小亚基
1.
The small subunit rDNA fragment of Comatricha nigra was amplified by using primers SMNUR101 (designed by Rusk et al in 1995) and NS4 (designed by White et al in 1990) The PCR product was cloned into E coli JM109 for sequencing The length of the sequence is 1 154bp The sequence was compared with that of Physarum polycepharum The results showed that the homology of these two species is 66
用Rusketal 于 1995年设计的引物SMNUR10 1和Whiteetal 1990年设计的引物NS4对黑发菌 (Co matrichanigra)的rDNA小亚基片段进行了PCR扩增 ,并将扩增产物克隆到大肠杆菌JM10 9中进行测序 ,测得的序列长度为 115 4bp。
3) SSU rRNA/rDNA
小亚基rRNA/rDNA
4) 5.8's rDNA-ITS gene sequence
5.8S rDNA-ITS基因序列
5) 18S rDNA sequence
18S rDNA序列
1.
The GenBank accession numbers of the 18S rDNA sequences of strain 7B3 is EU434621.
基于18S rDNA序列同源性比对以及系统发育树的分析,发现7B3是解脂耶罗威亚酵母。
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：N,N'-[亚乙基双(亚氨基亚乙基)]双二十二烷酰胺
CAS：72014-39-2
中文名称：N,N'-[亚乙基双(亚氨基亚乙基)]双二十二烷酰胺
英文名称：N,N'-[ethylenebis(iminoethylene)]bisdocosanamide
中文名称：N,N'-[亚乙基双(亚氨基亚乙基)]双二十二烷酰胺
英文名称：N,N'-[ethylenebis(iminoethylene)]bisdocosanamide
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条