Ribosomal RNA
- 网络核糖体RNA
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The Restriction Map of Ribosomal RNA Gene in Silkworm Attacus ricini
蓖麻蚕核糖体核糖核酸基因的限制性内切酶酶切图谱
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Preparation of Low - molecular Weight Ribosomal RNA from Chloroplast
叶绿体中低分子量核糖体RNA的制备
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A third class of RNA is also required for protein synthesis , the ribosomal RNA .
蛋白质合成还需要第三类RNA,即核糖体RNA。
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Direct Cloning of Bacterial Genes From Soil & 16S Ribosomal RNA Gene as a Model
土壤细菌基因资源的直接分离&16S核糖体RNA基因模式
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Study on the Sedimentation Coefficient of Ribosomal RNA from Saccharomyces cerevisiae
酿酒酵母菌核糖体RNA沉降系数的初步研究
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Application of ribosomal RNA gene ITS and IGS regions in the molecular identification and classification fungi
核糖体RNA基因间隔区ITS及IGS在真菌分子生物学鉴定和分型中的应用
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Studies on the control mechanism of genetic transcription during rat liver carcinogenesis & ⅱ comparison of ribosomal RNA
大鼠肝癌发生过程中基因转录调控机理的研究&Ⅱ.核蛋白体RNA的比较
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The detection of ribosomal RNA gene amplification during mouse oogenesis
小鼠卵子发生过程中核糖体RNA基因扩增的测定
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It will provide groundwork for the amplification of ribosomal RNA gene and sequence analysis . 2 .
为核糖体RNA基因序列扩增及序列分析奠定了基础。
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Erythrocytes recently released by the bone marrow into the bloodstream often contain ribosomal RNA .
刚从骨髓释放入血流不久的红细胞含有核蛋白体RNA。
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However , 18S ribosomal RNA ( rRNA ) usually be used as an internal control in real-time RT-PCR systems .
然而,在real-TimeRT-PCR体系中,18SRRNA也常被用作内参照。
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Nematode Diversity of Qingdao Coast Determined by PCR Retrieving and Sequencing of 18S Ribosomal RNA Gene Fragments
青岛沿岸自由生活海洋线虫18S核糖体RNA基因扩增及序列变异分析
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Analyses of small subunit ribosomal RNA sequence of the microsporidium , Nosema bombycis and its secondary structure
家蚕微粒子病原虫(NosemaBombycis)小亚基核糖体RNA全基因的克隆及其二级结构的构建
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However , false-positives can not be avoided when bacterial ribosomal RNA gene was amplified with universal primers .
但是,在使用通用引物扩增细菌基因时,假阳性很难避免。
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Objective : To determine whether there is ribosomal RNA genes ( rDNAs ) amplification during early mouse oogenesis .
目的了解小鼠卵母细胞成熟过程中是否有核糖体RNA基因(rDNAs)的扩增。
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Isolation and purification of 5S ribosomal RNA from the rhesus monkey ( macaca mulatta ) liver
猕猴(Macacamulatta)肝5S核糖核蛋白体RNA的分离提纯
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Bacterial 16S ribosomal RNA ( hereafter rDNA ) genes were PCR amplified from soil DNA , and cloned without artificial cultivation .
绕过细菌的分离培养,直接提取土壤DNA,扩增、克隆土壤细菌群体的16S核糖体RNA基因(16Srdna)。
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And ribosomal RNA ( rRNA ) has a structural role forming part of the ribosome & the machinery that converts RNA into protein .
核糖体RNA是核糖体结构的一部分,核糖体是使RNA翻译为蛋白质的机器。
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Characterisation of microsporidian species and differentiation among genetic variants of the same species has typically relied on ribosomal RNA ( rRNA ) gene sequences .
关于微孢子虫种的特征和相同种的遗传变异研究的经典方法都是利用核糖体RNA(rRNA)基因序列。
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Objective : To detect and observe types and transcription dynamics of small subunit ribosomal RNA ( SSUrRNA ) of Plasmodium berghei in Anopheles stephensi .
目的:观察伯氏疟原虫(P.berghei)小亚单位核糖体RNA(SSUrRNA)在斯氏按蚊体内的转录类型和动态。
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Chromosomal satellite & A small mass of chromatin containing genes for ribosomal RNA , at the end of the short arm of each chromatid of an acrocentric chromosome ;
染色质的一小部分,含有核糖体RNA基因,位于近端着丝粒染色体的短臂染色质末端;
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Cloning and Characterization of 18S 、 28S and 5.8S Ribosomal RNA Genes and Internal Transcribed Spacers of Seven Species / strains in Genus Prorocentrum
七种/株原甲藻的核糖体18S、28S、5.8S、ITS1和ITS2基因和区域的克隆与变异分析
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The application of molecular biotechnology such as molecule marker and the small subunit ribosomal RNA ( SSU rRNA ) in the research of ruminal protozoal was reviewed .
分子标记和基于小亚基核糖体RNA的分子生物学技术可以在基因和分子水平上为研究瘤胃原虫提供可靠而丰富的依据。
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Mitochondrial small subunit ribosomal RNA ( 12S rRNA ) gene has been used for phylogenetic analyses of a wide range of species and divergence levels for their universal occurrence , sequence and structure conservation and abundance .
12SRRNA基因由于其分布的普遍性、序列和结构的保守性以及进化速率镶嵌性而被广泛应用于不同分类阶元层次上的分子系统学研究。
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The ribosome-inactivating proteins ( RIPs ) from plants damage large ribosomal RNA of prokaryocyte or eukaryocyte , arresting the binding of ribosomes with elongation factors in translation , and inhibiting the protein synthesis .
植物核糖体灭活蛋白(ribosome-inactivatingproteins,RIPs)能够破坏真核或原核细胞的核糖体大亚基RNA,使核糖体失活而不能与蛋白质合成过程中的延伸因子相结合,从而导致蛋白质合成受到抑制。
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We examined the COI , nuclear genome ribosomal RNA spacer ( ITS ) and mitochondrial ribosomal large subunit ( 16S ) of three fragments in the molecular identification of Medusa as a means of effectiveness .
因此,本研究选取了COI、线粒体核糖体大亚基(16S)以及核基因组核糖体RNA间隔区(ITS)三种片段比较其作为水母类鉴定的有效性。