rna polymerase 中文意思是什麼

rna polymerase 解釋
rna聚合酶
  • rna : RNA =ribonucleic acid 【生物化學】核糖核酸。
  • polymerase : n. 【生物化學】聚合酶。
  1. Beta - exotoxin is an inhibitor of rna polymerase and acts competitively with atp in various biological processes

    外毒素是rna聚合酶的抑制劑,在各個生化過程中與atp起競爭作用。
  2. Eukaryotic messenger rnas are synthesized by the multisubunit enzyme rna polymerase ii, aided by myriad cofactors that control different events in this multistep process

    其mrna的合成是個多步驟的復雜過程,由控制該過程的多個輔因子協助rnap完成。
  3. The results of these early research work showed that rna polymerase transcription was localized in the nucleoli and rna polymerase and in the nucleoplasm

    當時的研究結果顯示: rna聚合酶的轉錄發生在核仁內, rna聚合酶和rna聚合酶的位於核質中。
  4. In recent years, more and more scientists presumed that rna polymerase transcription might not occur in the nucleoplasm but in the nucleoli. nevertheless, the possibility has not been proved directly

    近幾年,有許多學者相繼提出了rna聚合酶有可能在核仁區域內發生轉錄的觀點,但是這一觀點至今還沒有得到直接的實驗證據的支持。
  5. It is inferred that its active transcription occurs in the same region, not the nucleoplasm. the result will help us to further comprehend the mechanism of rna polymerase transcription, the way of its transcripts processing and transport, and the structural and functional relationship among the three rna polymeraes

    這一結果不僅直觀地向人們表明了rna聚合酶在真核細胞核中的轉錄位點,而且對於人們進一步認識和理解rna聚合酶的轉錄機制、其轉錄產物的加工運輸途徑、以及真核細胞當中不同的rna聚合酶間的組織和調控關系都將有著重要的理論意義。
  6. From these results, it is inferred that the active transcription of pol iii occurs in the nucleoli and its periphery region, but not the nucleoplasm. the result will help us to further comprehend the mechanism of rna polymerase iii transcription, the way of its transcripts processing and transport, and the structural and functional relationship among the three rnapolymeraes

    本實驗為rna聚合酶在真核生物細胞核中的轉錄位點提供了較為直接的證據,這對人們進一步了解rna聚合酶的轉錄機制、加工和運輸過程及三種rna聚合酶之間的結構與功能關系具有重要的意義。
  7. The results of these early research work showed that rna polymerase iii transcription was localized in the nucleoplasm. however, with the development and the application of new technologies since 1990s, the controversy arose on the transcription sites of rna polymerase iii. in recent years, more and more scientists presumed that rna polymerase iii transcription might not occur in the nucleoplasm but in the nucleoli

    自上個世紀八十年代初期,人們相繼運用細胞化學染色、電鏡放射自顯影等進行研究的結果表明: rna聚合酶的轉錄發生在核質中,但隨著新的研究技術的發展和應用,人們卻發現rna聚合酶的轉錄可能發生在核仁中,從而對早期的研究結果提出了質疑。
  8. The fragments were subcloned into a low copy transcription vector ( px8dt ) between the t7 rna polymerase promoter and autocatalytic hepatitis delta virus ribozyme. the result showed that genome of ndv f48e9 strain comprises 15192 nt, which was equal to zjl strain and 6 nucleosides longer than that of la sota, v4, bl and clone30

    實驗結果表明: f48e9全基因組具有15192個堿基,比lasota 、 v4 、 b1和clone30的全基因組序列長6個堿基,和鵝源zj1株的長度相等。
  9. Promotor, in broad sense, consists of transcription start site, binding site of rna polymerase ( promoter in narrow sense ) and upstream regulation sequence

    廣義的啟動子( promotor )包含有轉錄起始部位、 rna聚合酶與dna結合部位(也就是狹義的啟動子)以及上游調控序列。
  10. High stability of ptr102 - derived marking plasmids indicated that novel vector systems based on ptr102 could be constructed for the study on molecular biology and ecology of m. huakuii. 1kb gfp cdna fragment amplified by pcr was cloned into e. coli expression plasmid pet - hc, which was under the control of rna polymerase gene promoter from phage t7 with its own translation initiation codon

    將pcr擴增的1kbgfpcdna片段克隆到大腸桿菌表達載體pet - 11c上,使gfpcdna在帶有lac操縱基因的t7噬菌體rna聚合酶基因啟動子的控制下、以自身的atg作為翻譯起始密碼進行翻譯。
  11. Linearized full - length cdna was used as template then genomic rna of csfv was in vitro transcriped by t7 rna polymerase

    以線性化的全長cdna為模板,體外轉錄得到了csfv基因組rna 。
  12. A brief introduction to the x - ray crystallographic studies on rna polymerase complexes and the enzymatic mechanisms revealed by the crystal structures

    摘要用x射線晶體學方法測定的一系列rna聚合酶復合物結構揭示了真核轉錄的分子機制。
  13. It was showed under the laser scanning confocal microscopy that the transfected plasmid dna transcripted by rna polymerase and its transcripts were both localized in the interior and periphery of nucleoli

    由此我們認為rna聚合酶的轉錄就是發生在這一區域里,而並非是人們傳統認識中的核質中。
  14. Rna polymerase structure, bacterialrna

    聚合酶結構
  15. As rna polymerase ii leaves a gene promotor to transcribe the coding region, it faces many obstacles, including nucleosomes

    當rnap離開基因的啟動子轉錄編碼區時,遇到包括核小體在內的多種障礙。
  16. About 25 salt - induced proteins were identified by maldi - tof / ms, and finally the function of 17 induced proteins were determined, including heat - shock proteins ( groes, clp ). abc transporter, rna polymerase ( p - subunit ) and enzymes involved in signal transduction and metabolism. meanwhile, 84 proteins were idifferentially expressed after salt shock 5 min and 50 min in late exponential phase

    應用maldi - tof ms對30個鹽脅迫蛋白進行分析,已初步確定17個誘導蛋白的功能,其中包括與鹽脅迫相關的熱激蛋白( groes 、 clp ) 、與代謝途徑和信號傳導等有關的酶,以及abc轉運蛋白、轉錄調節蛋白、 rna聚合酶的亞基等。
  17. In this dissertation, the plasmids containing 5s promoter were transfected into cho cells and the transcription sites of rna polymerase and its transcripts were detected by fluorescence in situ hybridization to dna and rna, respectively

    本實驗以中國倉鼠卵巢細胞( cho )為實驗材料,利用基因轉染、熒光原位雜交並結合激光共聚焦顯微鏡觀察的方法,在dna和rna水平上分別對rna聚合酶的轉錄位點和轉錄子的分佈進行了檢測。
  18. Streptomyces whig gene is a key gene encoding a development ally important rna polymerase sigma factor ( awhig ), which specifically initiates development program and determines the developmental fate of the cell

    Whig基因編碼一個發育上重要的rna聚合酶因子,特異性地起始發育程序,決定菌絲細胞的發育命運。
  19. In this dissertation, the plasmids containing 5s promoter were transfected into hela cells, the transcription sites of rna polymerase iii and its transcripts were detected by fluorescence in situ hybridization ( fish ) to dna, rna and dna - rna, respectively

    本實驗以人的hela細胞為材料,運用電擊轉染、熒光原位雜交並結合激光共聚焦顯微鏡,從dna 、 rna和dna - rna三個水平對rna聚合酶的轉錄位點及其轉錄子的分佈進行研究。
  20. After the statistical analysis on the distances between different particles representing baf complex, nf1 / ctf and polymerase ii large subunit, respectively, we further proved that the baf complex is closely associated to nf1 / ctf and rna polymerase ii large subunit. but nf1 / ctf and rna polymerase ii are weakly associated

    通過計算和分析分別代表兩種蛋白質的兩種金顆粒之間的距離,進一步證實baf復合物與rna聚合酶11的大亞基及轉錄因子呷ctf之間的聯系緊密,而轉錄因子nfi ctf與叫a聚合酶11的大亞基之間的聯系相對較弱。
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