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1.Assay of Genomic DNA Homology Among & Candida Species by Total Chromosome DNA Hybridization
全染色体DNA杂交技术分析八种念球菌基因组DNA同源性收藏指正
2.ETERMINATION OF DNA G+C mol% AND DNA HOMOLOGY BETWEEN EXTRA-SLOW-GROWING SOYBEAN RHIZOBIA AND OTHER RHIZOBIA
超慢生大豆根瘤菌DNA G+C含量和DNA同源性测定收藏指正
3.The DNA G+C mol% for extra-slow-growing soybean rhizobia (ESG) and DNA homology for ESG strains and other rhizobia were carried out by thermal denatu-ration temperature (Tm) and reassociation rate of DNA, respectively.
用热变性温度法和液相复性速率法分别测定了超慢生大豆根瘤菌(ESG,extra-slow-growing soybean rhizobia)DNA G+C mol%及与其它根瘤菌间的DNA同源性.收藏指正
4.The SDS-PAGE electropheresis of whole-cell proteins was applied in classification of 71 strains isolated from Astragalus spp..It was showed that the technique is a simple and rapid method in classification of rhizobia.The similarity of strains in the same group is 78%,and DNA homology is above 70%.
采用SDS-PAGE技术对71株黄芪根瘤菌进行了全细胞蛋白的聚类分析.结果表明,这是进行根瘤菌分类时一种简便快速的分群方法,分群的菌株相似性水平为78%,群内菌株的DNA同源性70%.收藏指正
5.soja was 59. 2-63. 5% and the DNA homology among five representative strains of ESG was greater then 7 0 % ( range ,72. 1 to 93. 4%), which indicated that these strains were in one genetic group. (2) DNAs from 5 ESG representative strains had very low mean homology (range,3. 8 to 30. 0%) with 16 other reference rhizobial strains.
ESG与在大豆上结瘤的快生大豆根瘤菌(Rhizobium fredii USDA205)同源率为14.8%,与慢生大豆根瘤菌(Bradyrhizobiumjaponicum)三个DNA同源组的同源率分别为20.5%,30.0%,19.4%.收藏指正
6.The homology of this gene was 98% with human chromosome 1p36.2-36.3 DNA sequences,the homology of this gene coding protein was 85% with Alu subfamily SB sequence.
核酸同源性比对发现与人类1p36.2鄄36.3染色体DNA序列同源性达98%,编码蛋白质同Alu亚家族SB序列同源性达85%。收藏指正
7.But the comparison amino acid sequence shows that GPV DNA has high homology with the human adeno-associated virus AAV-2 in dependovirus and B19 in erythrovirus.
GPV与依赖病毒属成员AAV-2及红病毒属成员人细小病毒B19的进化关系较近。收藏指正
8.In the 1.2 kb fragment, there were also several conserved motifs such as CAAT-box and GAGA-box, which are related to regulation of transcription, and the putative binding sites of transcriptional factors such as EBP, EFII, NF-E1and LV. The results of BLAST showed that the DNA sequence shared high homology with the 5′-upstream region of Dunaliella viridis NR genome.
该序列含有多个与转录调控有关的保守序列(如CAAT-box和GAGA-box),含有与EBP、EFII、NF-E1、LV等转录因子以及广谱激活剂Oct-1结合位点相似的核苷酸序列。收藏指正
9.Y4 fragment was cloned into a PMD18-T vector and the nucleotide sequence determined. Partial sequencing of the CPV-VP2-Y3? Y4 DNA fragment showed 99% nucleotide homology with that of the canine parvovirus,strain CPV/HN-1.
将分离到的犬细小病毒VP2 Y34基因片段克隆到PMD1 8 T载体 ,其病毒基因组CPV VP2 Y34序列测定结果显示与作者在GENEBANK发表的肺病变犬细小病毒CPV HN 1株有 99%同源性收藏指正
10.The DNA sequence of the cloned NS1 gene showed a 99%homology with the DEN2 NGC(Genbank:AF038403).
序列测定证实该基因与DEN2(NGC株AF038403)NS1基因序列有99%同源。收藏指正
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