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   regulation region 在 生物学 分类中 的翻译结果: 查询用时:0.57秒
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regulation region
相关语句
  调控区
    Conclusion The target fragments of SCN5A intron 1 have strong activity of transcriptional regulation in HEK293, a positive regulation region exists between +329 bp and +385 bp in intron 1, and the region can be bound by MZF1, USF and C-ETs-1 which might be involved in the positive gene regulation.
    SCN5A基因+329 bp~+385 bp为正调控区,软件分析MZF1、USF、C-ETs-1等因子能与这些正调控区域结合并可能参与SCN5A基因的表达调控。
短句来源
    Probable Existence of a Negative Regulation Region Within the 3′UTR of Human Phosphoinositide 3-Kinaseγ mRNA
    PI3KγmRNA 3′非翻译区可能存在基因表达负调控区
短句来源
    Identification of binding protein to a 30 bp-negative regulation region upstream of NKX 3.1 gene
    NKX3.1基因上游一个30bp负调控区结合蛋白的初步鉴定
短句来源
    The bovine aS1-casein 5'regulation region about 2.08Kb and 3'flanking region about were got by PCR.
    利用PCR反应,分别扩增出了牛αS1—酪蛋白的5’调控区约2.08Kb和3’侧翼区约2.76Kb。
短句来源
    Firstly, the bovine aS1-casein 5'regulation region was cloned into the vector pEGFP-1 and constructed a new vector P-5;
    首先将牛αS1—酪蛋白的5’调控区克隆到载体pEGFP-1上,成为载体P-5;
短句来源
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  调控区
    Conclusion The target fragments of SCN5A intron 1 have strong activity of transcriptional regulation in HEK293, a positive regulation region exists between +329 bp and +385 bp in intron 1, and the region can be bound by MZF1, USF and C-ETs-1 which might be involved in the positive gene regulation.
    SCN5A基因+329 bp~+385 bp为正调控区,软件分析MZF1、USF、C-ETs-1等因子能与这些正调控区域结合并可能参与SCN5A基因的表达调控。
短句来源
    Probable Existence of a Negative Regulation Region Within the 3′UTR of Human Phosphoinositide 3-Kinaseγ mRNA
    PI3KγmRNA 3′非翻译区可能存在基因表达负调控区
短句来源
    Identification of binding protein to a 30 bp-negative regulation region upstream of NKX 3.1 gene
    NKX3.1基因上游一个30bp负调控区结合蛋白的初步鉴定
短句来源
    The bovine aS1-casein 5'regulation region about 2.08Kb and 3'flanking region about were got by PCR.
    利用PCR反应,分别扩增出了牛αS1—酪蛋白的5’调控区约2.08Kb和3’侧翼区约2.76Kb。
短句来源
    Firstly, the bovine aS1-casein 5'regulation region was cloned into the vector pEGFP-1 and constructed a new vector P-5;
    首先将牛αS1—酪蛋白的5’调控区克隆到载体pEGFP-1上,成为载体P-5;
短句来源
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  “regulation region”译为未确定词的双语例句
    The Study on the 5 Flanking Regulation Region of the Human Vigilin Gene
    人vigilin基因5'端调控区域的研究
短句来源
    Polymorphsim analysis of the regulation region of human tissue kallikrein gene in Chinese Han Race
    汉族人群组织激肽释放酶基因调控序列多态性分析
短句来源
    Analysis of the 5' deletion constructs showed the regulation region of its basic transcription was mainly within - 1520 to - 1431 bp upstream of ATG Two stem-loop structures were within - 1108 to - 1079 and - 891 to - 864 bp relative to ATG It suggests that their protein binding site is between - 1079 to - 897 bp relative to ATG.
    利用DNAMAN软件分析,在-1108至-1079bp和-891至-864bp之间存在着两个茎环结构,推测茎环结合蛋白位点可能位于-1079至-897bp之间,且ATG上游-388至-86bp之间可能存在乙酰苯胺类化合物诱导元件。
短句来源
    The 5′regulation region was about 2 826 bp, and consisted of
    长 2 826 bp,包括 1.7 kb 的上游调控序列以及 5'不翻译区的第一外显子和部分第一
短句来源
    Methods:Following the report gene containing different regulation region of TNF-α gene transfected into HL-60 cell,its expression level stimulated with/without LPS or blocked with κB 3 antisense was detected respectively;
    方法 :用含不同调节区域的重组报告基因进行HL 6 0细胞的基因转染 ,检测LPS刺激前后及κB3 反义寡核苷酸封闭后的报告基因表达水平 ;
短句来源
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  regulation region
A site-directed mutant DNA fragment was synthesized and transfected into clinical Neisseria Gonorrhoeae (NG) stains to construct the transformants that contained the corresponding mutagenesis of regulation region of mtrR gene.
      
In vitro recombination and identification of mutated fragment corresponding to regulation region of mtrR gene of Neisseria Gonor
      
The mutation (C→T) in the 5' regulation region of chicken MC4R gene results in one more NF-E2 and cap transcription factor binding sites in the mutation allele than in the wild allele.
      
Unusual structure in the regulation region of the Bacillus subtilis riboflavin biosynthesis operon.
      
The genes of most of the structural muscle proteins have a MyoD-binding regulation region.
      
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Attacus ricini is a species of insect which only grows in China. It is expected to construct a new expression system for genetic engineering by using ArNPV as a vector. We have established an ArNPV gene library. The 1.1 kb DNA fragment containing ArNPV Ph gene was subcloned. Sequencing analysis showes that the 735 bp Ph structural gene has the homology of 76% and 81% with those of AcNPV and BmNPV respectively. The Rohrmann box in the ArNPV 5'-end regulation region is very similar to those of various other...

Attacus ricini is a species of insect which only grows in China. It is expected to construct a new expression system for genetic engineering by using ArNPV as a vector. We have established an ArNPV gene library. The 1.1 kb DNA fragment containing ArNPV Ph gene was subcloned. Sequencing analysis showes that the 735 bp Ph structural gene has the homology of 76% and 81% with those of AcNPV and BmNPV respectively. The Rohrmann box in the ArNPV 5'-end regulation region is very similar to those of various other NPVs, but the 3'-end downstream sequence has almost no homology with those of AcNPV and BmNPV, demonstrating the characteristic property of the structure of ArNPV Ph gene. Other structural features of the Ph gene promoter are also discussed in this paper.

蓖麻蚕(Attacus ricini)是我国特有蚕种,以其核多角体病毒(ArNPV)为载体有可能发展成为新的基因工程表达系统,我们建立了ArNPV基因库,并亚克隆了含多角体蛋白(Ph)基因DNA片段。对该1.1kb全长DNA片段进行序列分析,确定ArNPV Ph结构基因全长735bp,与苜蓿尺蠖NPV(AcNPV)、家蚕NPV(BmNPV)同源性分别为76%和81%,ArNPV 5'端调控结构Rohrmann box与各类NPV的Ph基因相似,但3'下游序列几无同源,显示了ArNPV Ph基因结构的特征性。同时,我们还对Ph基因启动子的其它结构特点作了剖析。

By the PCR method, the main domains of two mutants of Drosophila zip gene (zipID16 and have been amplified and cloned for DNA sequencing. The results showed that no expected mutant site was found within the amplified DNA fragments, indicating that the possible spot-mutant site may be located in either the signal peptide part or the regulation regions. Thus, there will be some single key animo acid or important base site in these two regions.

本文利用PCR技术对两个果蝇突变株zip~(ID16)、zip~(IIF107)的突变zip基因的主要结构域部分进行了扩增,并在克隆后作序列分析。排除了突变发生在这些区域的可能性,表明可能的突变位点:一是位于信号肽部分,二是处于调控区。提示在这两个区域可能有关键性的单个氨基酸或单个碱基位置的存在。

The gene,coding for a new protein called vigilin,was isolated from chicken chondrocytes.Vigilin mRNA exists in two size species(4.4 kb and 6.5 kb).The vigilin gene is expressed in human tissue too.For further exploring the transcription starting site and regulatory element of human genomic vigilin gene.5 flanking EcoR Ⅰ fragment(Vig CG5 7E)was subcloned from a genomic DNA and selected 6 corresponding enzymes to establish the restriction map.Meanwhile,the...

The gene,coding for a new protein called vigilin,was isolated from chicken chondrocytes.Vigilin mRNA exists in two size species(4.4 kb and 6.5 kb).The vigilin gene is expressed in human tissue too.For further exploring the transcription starting site and regulatory element of human genomic vigilin gene.5 flanking EcoR Ⅰ fragment(Vig CG5 7E)was subcloned from a genomic DNA and selected 6 corresponding enzymes to establish the restriction map.Meanwhile,the locality of transcription starting site and sequence analysis of regulation region of the human vigilin gene was described.After the clone Vig CG5 7E being completely digested with the restriction enzyme Apa Ⅰ,they were electrophoretically separated and transfered onto a nitrocellulose filter,and were hybridizated with a 20 bp probe from the cDNA .The length of hybridization area was 0.1kb.It located at of the out Apa Ⅰ end of Vig CG5 7E3AE.It is shown that clone Vig CG5 7E3AE include regulation elements of the vigilin gene by sequencing analysis.Two TATA box,one CAAT box and one GC box and two consensus sequences of Ap 1 and Ap 2 was found in the area.It was predicted that GC box is a promoter element of vigilin gene.

在克隆了人基因组全长vigilin基因的基础上,对其5端转录调控区域再克隆,获得Vig-CG5-7E克隆,再用限制酶ApaⅠ和EcoRⅠ切除3端约4kb部分,得到Vig-CG5-7E3AE克隆,并对该克隆进行双向测序分析.结果表明:克隆Vig-CG5-7E用ApaⅠ酶消化后,用cDNA上游开始的20个碱基组成的寡聚核苷酸做探针进行分子杂交,可见一条小于0.1kb杂交带,根据物理图谱分析,位于Vig-CG5-7E3AE克隆的ApaⅠ端,从而推断该克隆含有转录调控元件,5端序列分析得到二个TATA盒,一个CAAT盒和一个GC盒以及二个可能的Ap-1和Ap-2结合位点.认为GC盒可能为人vigilin基因启动子的组成部分

 
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