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诱导调控
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  “诱导调控”译为未确定词的双语例句
     Results p4COL1A2-d2EGFP was the better smad3-responsive d2EGFP reporter gene system and the smad3 TFD could antagonize the d2EGFP expression induced by TGF-β1 significantly.
     结果:NIH3T3-d2EGFP是较理想的Smad3反应性报告细胞株,Smad3TFD对TGF-β1诱导调控d2EGFP的表达具有明显的拮抗作用。
短句来源
     A Study on Regulating Bax Expression by Radiation-inducible Egr-1 Promoter
     Egr-1启动子放射诱导调控Bax基因表达的研究
短句来源
     There are several conserved sequences in promoter region of SP1 and SP2, such as sucrose box,CAAT box and TATA box.
     在SP1和SP2 的基因启动子区都存在几种典型的保守序列, 如受糖诱导调控的蔗糖盒(Suc-box),CAAT盒和TATA盒。
短句来源
     With the cotransfection of NF- κB transcription factor decoy (TFD) and p65 vector into HEK- d2EGFP cells, the results showed the groups of 1 mg/L and 2 mg/L TFD could antagonized the d2EGFP expression induced by p65 protein significantly.
     应用NF κB“圈套”寡核苷酸 (TFD)与 p6 5载体瞬时共转染HEK d2EGFP ,1mg/L NF κB和 2mg/LNF κBTFD组对p6 5蛋白诱导调控表达的d2EGFP具有明显拮抗作用 .
短句来源
     [Methods] The entire MSP1 gene and 42 kDa fragment gene were cloned into the plasmid of pZE11,and transformed into E coli DH5αZ1. Restriction e nzyme analysis, SDS-PAGE and Western blotting were used to examine two recombinant plasmids and their expression in E coli DH5αZ1. [Results ] The recombinant plasmids of pZE11/MSP1 and pZE11/MSP1-42 were constructed successfully.
     [方法 ]将MSP1全合成基因和MSP1C末端 42kDa片段基因分别克隆入受四环素诱导调控的质粒pZE11上 ,转化大肠杆菌DH5αZ1,质粒经酶切、SDS PAGE电泳和Westernblotting反应鉴定重组质粒的构建和重组质粒在DH5αZ1中的表达。
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     Regulation of RFP13 Induced Apoptosis
     RFP13诱导细胞凋亡的调控
短句来源
     Cold-induced Apoptosis and Its Modulation Mechanism
     冷诱导细胞凋亡及其调控机制
短句来源
     regulate and control the enterprise groups with state policy;
     国家政策调控 ;
短句来源
     in troducing stimulus;
     诱导刺激;
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     third,self-regulation.
     自我调控
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  inducible regulation
Nuclear factor-κ B (NF-κB)/Rel transcription factors play an important role in the inducible regulation of a variety of cytokine genes in epithelial cells.
      
The application of an inducible regulation system using the trytophanase operon promoter (TPase promoter; Ptna) was examined for its high expression of the tryptophan synthase (TS) gene in Escherichia coli.
      
The inducible regulation is independent of the promoter that is used to activate cat-86 and is independent of the cat-86 coding sequence.
      
In this review, we will discuss the current knowledge regarding the DNA elements and protein factors involved in both constitutive and inducible regulation of Pgp transcription in normal and tumor cells.
      
These genes are developmentally regulated with constitutive expression in mature B cells and inducible regulation in a variety of cell types.
      


Two pairs of primers were synthesized on the basis of known promoter sequences of sweet potato storage protein (sporamin) and two kinds of DNA fragments were obtained by using polymerase chain reaction from Ipomoea batatas cv.Nanshu 88 genome. One of the fragments (called SP2) contains both sequences of promoter and ribosome binding site (RBS),while the another fragment (called SP1) contains not only promoter and RBS but also the signal peptide coding sequence. DNA sequence analysis showed that SP1 and...

Two pairs of primers were synthesized on the basis of known promoter sequences of sweet potato storage protein (sporamin) and two kinds of DNA fragments were obtained by using polymerase chain reaction from Ipomoea batatas cv.Nanshu 88 genome. One of the fragments (called SP2) contains both sequences of promoter and ribosome binding site (RBS),while the another fragment (called SP1) contains not only promoter and RBS but also the signal peptide coding sequence. DNA sequence analysis showed that SP1 and SP2 had high sequence homology (82%) in the promoter and RBS region. There are several conserved sequences in promoter region of SP1 and SP2, such as sucrose box,CAAT box and TATA box.Two specific expression vectors were constructed by using these two fragments for foreign genes expression in sweet potato.

根据已知的甘薯块根贮藏蛋白基因序列, 设计和合成了两对PCR引物。用PCR方法,从南薯88基因组中分别扩增出两种DNA片段: 一种含有贮藏蛋白基因启动子和核糖体结合序列(SP2);第二种不仅含有第一种DNA片段的全部序列,而且还有贮藏蛋白的信号肽编码序列(SP1)。核苷酸序列分析表明,这两种DNA片段的启动子和核糖体结合区虽然具有很高的同源性(82% ), 但它们并不相同。在SP1和SP2 的基因启动子区都存在几种典型的保守序列, 如受糖诱导调控的蔗糖盒(Suc-box),CAAT盒和TATA盒。用这两种DNA片段分别构建了可调控的甘薯高效表达载体。

The advances on cell locations, basic properties, inductions, gene expression and regulation of phenylalanine ammonia-lyase (PAL) and its role in plant disease resistance were reviewed in detail in the paper.

对苯丙氨酸解氨酶的定位、基本特性和诱导调控及其在植物抗病反应中的作用等方面的研究进展进行了较全面的综述

The Hybrid gene SA 28 coding for a modified Hepatitis B surface antigen and preS1 epitope was inserted into EcoRⅠ site of highly stable plasmid pAO815. The SA 28 gene in pAO815 was under the control of the methanol inducible alcohol oxidase(AOX1) promoter. Linearized pPFD1 were transformed into a proteinaseA deficient strain SMD1168 of P. pastoris yeast and integrated in the chromosomal 5' AOX locus forming a homologous recombination. The results showed the expression of SA 28 gene was regulated by methanol...

The Hybrid gene SA 28 coding for a modified Hepatitis B surface antigen and preS1 epitope was inserted into EcoRⅠ site of highly stable plasmid pAO815. The SA 28 gene in pAO815 was under the control of the methanol inducible alcohol oxidase(AOX1) promoter. Linearized pPFD1 were transformed into a proteinaseA deficient strain SMD1168 of P. pastoris yeast and integrated in the chromosomal 5' AOX locus forming a homologous recombination. The results showed the expression of SA 28 gene was regulated by methanol and the expression product contains both HBsAg and preS1 antigencity.

将乙肝病毒表面抗原S preS1融合基因SA 2 8插入质粒载体 pAO815的EcoRⅠ位点中 ,将其置于PichiaPastoris酵母AOX1启动子控制下 .利用电转化技术 ,融合基因表达单元连同HIS4基因被整合到受体菌SMD116 8基因组中 .对得到的工程菌进行发酵和表达产物的研究表明 :SA 2 8基因在该系统中的表达受甲醇诱导调控 ;SA 2 8融合基因的表达产物具有S和PreS1的双重抗原性 .用CsCl密度梯度离心法纯化了表达产物 ,融合抗原活性峰位于密度为 1 19mg/cm3 的区带 .

 
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