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The fluorescence spectra of 9-(3-aminoanilino)acridine(B2,m-APAA) with Deoxyribonucleic acid(DNA) has been studied, so a fluorescent method for the determination of DNA was established;
中文意思:
对9-(3-氨基苯胺基)吖啶(B_2,简称m-APAA)与脱氧核糖核酸(DNA)作用的荧光光谱进行了研究,拟定了测定DNA的分析方法,探讨了反应机理,实验了最佳条件、干扰实验。


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The expressions of cytokines essential for the growth of hEG,namely basic fibroblast growth factor(bFGF) and leukemia inhibitory factor(LIF),were also examined by RT-PCR. 应用RT-PCR检测hEG生长所需的重要细胞因子的表达,即碱性成纤维细胞生长因子(bFGF)和白血病抑制因子(LIF)。
The extraction of nucleic acid is the foundation in molecular biological experiments, and RNA with high quality is the premise for cDNA library construction and genes expression. 核酸提取是分子生物学实验的基础,提取高质量的核糖核酸(RNA)是构建cDNA文库和进行基因表达研究工作的前提。
The feasibility to improving rooting ability and topical dominance with both rolB and pttGA20ox genes at the same time was proved by transforming mode plant tobacco. 通过转化模式植物来验证同时转化rolB及pttGA20ox两个基因促进植物生根及顶端优势的可行性。
The fingerprintings were more clearer when the genome DNA was 100ng/μl. 白色念珠菌基因组DNA含量在100ng/μl时,得到的指纹图谱最为清晰;
The first group included 19 cases with fatty liver(38.78%); the second group included 29 cases without fatty liver(61.22%). Blood lipids in 2 groups were analyzed with biochemical method. 所有患儿分为脂肪肝组19例(38.78%)及无脂肪肝组29例(61.22%),对2组血脂成分进行分析。
The fluorescence spectra of 9-(3-aminoanilino)acridine(B2,m-APAA) with Deoxyribonucleic acid(DNA) has been studied, so a fluorescent method for the determination of DNA was established; 对9-(3-氨基苯胺基)吖啶(B_2,简称m-APAA)与脱氧核糖核酸(DNA)作用的荧光光谱进行了研究,拟定了测定DNA的分析方法,探讨了反应机理,实验了最佳条件、干扰实验。
The four enzyme s belonging to classⅠ,ADH,HK,PFK and PDC,all catalyze irreversible reaction s. 属于第一大类的四种酶ADH、HK、PFK和PDC,均催化不可逆反应。
The function of antisense PIP RNA on HBV PRE-dependent post-transcriptional regulation PIP反义核酸对乙肝病毒PRE转录后调节的影响
The fusion protein was soluble and over 30% of the total protein in the supertanant after ultrasonication . 表达的融合蛋白主要以可溶形式存在于宿主细胞内,超声破菌后,融合蛋白的含量占上清蛋白总量的30%以上。
The gene chip used in this study contained 407 genes. 本研究还针对407个基因(包括信号传导有关的基因及转录因子)制备了基因芯片。
The genotypes of their serum HBV were detected by using PCR integrated with Tagman MGB probe technology, and their serum HBV markers, HBV DNA and liver functions were also examined. 采用PCR结合Taqman MGB探针技术,对血清中HBV基因型进行分型检测,同时检测HBV血清标志物、HBV DNA、肝功能。
 
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