轉錄區 的英文怎麼說

中文拼音 [zhuǎnlùqū]
轉錄區 英文
transcriptional domain
  • 轉 : 轉構詞成分。
  • 錄 : Ⅰ名1 （用做記載物的名稱） record; register; collection; selections 2 （姓氏） a surname Ⅱ動詞1 （...
  • 區 : 區名詞（姓氏） a surname
  • 轉錄 : [電學] transcribe; transfer; [聲學] mixing; rerecording; [生物學] transcription; duplicating轉錄...
  1. Sequence differences of second internal transcribed spacer of ribosomal dna in anopheles minimus

    內轉錄間隔2區序列差異
  2. Constructing quantitative model with ordinary differential equations for the cell - cycle control system, it is appropriate to use ordinary differential equations ( odes ), because molecular diffusion, transcription, translation and membrane transport seem to be fast ( a matter of seconds ) compared with the duration of the cell cycle ( hours ). spatial localization of reactions can be handled by compart - mental modelling, in the spirit of pharmacokinetics

    對于這樣的細胞周期控制系統，應用常微分方程是適合的，因為比起細胞周期的時間（以小時計）來，分子擴散，轉錄，翻譯和膜運輸是很快的（以秒計應用藥物動力學的區域化模型的方法，可以處理反應的空間分佈。
  3. Some tendency of tn5gusa5 transposition were found that all preferred sites of tn5gusa5 in xcc 8004 genomic dna are in at - rich regions ; target sequences of tn5gusa5 have some features that the probabilities of guanine and cytosine are high respectively at the head and tail base of target sequence ; the level of gene transcription does not influence insertion density of tn5gusa5 significantly

    結果表明， tn5gusa5插入位點有一定的規律性： tn5gusa5在xcc8004基因組上傾向于插入低gc含量（ 50左右的區域插入密度最高）區段；插入位點的靶序列有一定的特異性，在靶序列的首位鳥嘌呤出現的幾率高，而在靶序列的末位胞嘧啶出現幾率高； tn5gusa5的插入密度與該區段基因的轉錄水平無明顯關系。
  4. Notch interaction with its ligands induces the cleavage of its intracellular domain ( ic ), and the notch ic translocates to the nucleus and binds to rbp - j, the mammalian homolog of su ( h ), to transactivate transcription of target genes such as e ( spl ) ( enhancer of split ), hesl ( hairy and enhancer of split ) and hes5 four notch receptors and their ligands are differentially and redundantly expressed in a variety of vertebrate tissues

    它通過其識別序列（ cogtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。在沒有n 。 tch胞內段的情況下， rbpj可與包含sm盯（ silencingmediatorforretlnoldandthyroidhormonereceptor ）和組蛋白去乙酞化酶的轉錄輔助抑制復合物結合，當notch信號被激活時； rbpj可與n 。
  5. The two single - pass transmembrane proteins, delta and serrate, have been identified as notch ligands. the transcription factor suppressor of hairless [ su ( h ) ] is the major downstream effector of notch signaling pathway. rbp - j, the mammalian homolog of su ( h ), recognizes the core sequence ( c / tgtgggaa ) of dna

    Rbp - j是果蠅促神經發生基因su （ h ） （ suppressorofhairless ）在哺乳動物的同源物，它通過其識別序列（ c tgtgggaa ）結合於受調控基因的啟動子區，在轉錄激活因子的驅動下調節細胞分化和個體發育相關基因的表達。
  6. To test the p7 promoter activity, a series of constructs were obtained by cloning the different dna fragments into the luciferase gene reporter vector pgl3 - b. when the constructs were transiently transfected into thp - 1 cells, luciferase activity assay showed that the core region of p7 promoter located at - - 165 bp

    第一部分的工作首先通過對人acat - 1基因p7啟動子序列進行5 '和3 ' -端的缺失的詳細分析，結果顯示最大報告基因轉錄表達活性位於- 612 - 165bp區段。
  7. 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。
  8. It was showed under the laser scanning confocal microscopy that : for dna level fish, 81 % of the dnas were in the nucleoli and at the periphery of the nucleoli and 19 % in the nucleoplasm ; for rna level fish, 22 % of the rnas were in the nucleoli, 78 % in the nucleoplasm and at the boundary between it and the nucleoli ; for dna - rna level fish, 25 %, 46 % and 29 % of the dnas or rnas were in the nucleoli, at the periphery of the nucleoli and in the nucleoplasm, respectively

    結果如下： dna水平熒光原位雜交結果顯示， 81的dna位於核仁內部及其核仁周邊區域， 19的位於核質中； rna水平熒光原位雜交結果表明， 22的rna位於核仁內， 78的位於核質及與核仁交界處； dna - rna水平熒光原位雜交結果是， 25的dna或rna位於核仁內， 46處于核仁周邊， 29位於核質中。由此推測出， rna聚合酶的轉錄主要發生在核仁及其周邊區域。
  9. This uncoiled condition is thought to facilitate transcription and probably indicates an area where genes are active

    解聚的狀態可以幫助轉錄的完成，預示著這個區域內的基因是活躍的。
  10. Culture of mg7 hybridoma cells and detection of antigen - binding affinity of mg7 mab by elisa 2. construction and identification of mg7 recombinant phage antibody library mrna was isolated from cultured mg7 hybridoma cells and converted into cdna ; the variable fragments of heavy and light chain were separately amplified and assembled into scfvs with a specially constructed dna linker by pcr. the scfvs dma was ligated into the phagmid vector pcantabse and the ligated sample was transfered into competent e. co / / tg1 to generate a bacterial form of mg7recombinant phage antibody library ; volume and recombinant ratio of the library were evaluated by means of bacterial colony counts and restriction analysis ( ecor i and hind iii )

    Mg _ 7重組噬菌體抗體庫的構建及鑒定從培養的mg _ 7雜交瘤細胞中提取並分離mrna ，反轉錄成cdna ；利用pcr分別擴增mg _ 7單抗的重鏈及輕鏈可變區基因，並通過? dna連接子將二者連接起來形成mg _ 7單鏈抗體基因；將mg _ 7單鏈抗體基因插入pcantab5e ；將連接產物轉化感受態tg1大腸桿菌，制備細菌形式的mg _ 7重組噬菌體抗體庫；通過菌落計數和限制性酶切分析（ ecor和hind ）評估mg _ 7重組噬菌體抗體庫的容量和重組率。
  11. Based on the deletion region, the possible candidate genes of 20 stocks were searched in flybase. they mainly function as transcription factors, tran slation factor, kinase, signal molecules, and so on

    根據缺失區段，在果蠅數據庫中檢索了7個品系相關的可能候選基因，它們的功能主要有轉錄因子、翻譯因子、激酶、和信號分子等。
  12. But polyadenylation in bacteria needs no specific consensus sequence or there is no such sequence signals found. the sites of polyadenylation of bacterial mrna are diverse, including the 3 ' ends of primary transcripts, the sites of endonucleolytic processing in the 3 ' untranslatd and intercistronic regions, and sites within the coding regions of mrna degradation products

    細菌mrna多聚腺苷酸化的位點多種多樣，包括初級轉錄產物的3 』末端， 3 』端非翻譯區和順反子間區的內切酶加工位點及mrna降解產物的編碼區內，其腺苷酸化相對無特異性、無選擇性。
  13. The ir sequence of mxmybl is most homologous with that of atmyb ( 86. 9 % ) and somewhat homologous with that of stmyb 1 ( 77. 0 % ) ; there is very low homology among n - and c - terminal regions outside of the ir regions of all of the mybs ; the protein mxmybl contains a proline - rich region as well as a serine - rich region near the c - terminus, such structure motifs are implicated in transcriptional activation

    9 ，與馬鈴薯stmyb的ir序列的同源性達77 0 ，所有這些nnrb蛋白除了瓜區具有較高的同源性外，其c端和n端幾乎沒有同源性。 mwyb蛋白的c一端還含有一個富含脯氨酸區，這樣的結構基序可能具有激活轉錄的功能。
  14. 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。
  15. In order to study the expression of 3 - defensins in liver as acute phase response proteins, a murine systemic acute phase responsive model was established by intraperitoneal injection o f lipopolysaccharide ( lps ) in our study. the mbd3 cdna sequence ( 145 - 169 bp ) was labled with [ - 32p ] atp as a probe to detect mbd3 mrna in different tissues by northern blot and analyze the time - and dose - dependant expression caused by lps. the 5 " flanking sequence ( - 167 - 179 bp ) of the mbd3 gene was designed as the probe and labled with [ - 32p ] dctp to investigate the binding of transcriptional factors to this region by electrophoretic mobility shift assay ( emsa ) and south - western blot

    以小鼠mbd3基因145 ? 169bpcdna序列合成探針，經[ - ~ （ 32 ） p ] atp標記后通過northernblot方法檢測mbd3在肝臟中的表達，同時分析了mbd3基因誘導表達的組織特異性，劑效和時效關系；結合mbd3基因啟動子區序列分析，以- 164 ? - 179bp雙鏈dna序列合成探針，經[ - ~ （ 32 ） p ] dctp標記后通過電泳遷移率改變實驗（ emsa ）和south ? westernblot方法對參與mbd3在肝臟中誘導表達調節的轉錄因子進行分析。
  16. Acbf is a transcription factor that combined with the ac - rich region of the promoter region. it has been cloned at arabidopsis thaliana, nicotiana tabacum and so on

    Acbf編碼了結合在苯丙氨酸解氨酶啟動子ac富集區上的一個轉錄因子， acbf基因已經在擬南芥、煙草等植物中得到了克隆。
  17. Abstract : the nucleosome, the structural unit of chromatin, is known to play a central role in regulating gene transcription from promoters

    摘要：核小體作為染色質的結構單位，在基因啟動子區域調節基因轉錄中具有重要的作用。
  18. 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。
  19. Two strains of prrsv were isolated from the swine infected with prrsv in shangdong province and daqing area, in order to clarify the source and genetic background of porcine reproductive and respiratory syndrome virus ( prrsv ) from different parts of china, thus providing theoretic basis for the study of vaccine against it. the prrsv was cultured on mark - 145 cells for 5 ~ ~ 6 passages. when the cpe was obvious, the virus was harvested and purified

    為了弄清我國不同地區prrsv的來源以及其遺傳學背景，為疫苗學研究提供理論根據，本研究在ch - 1a株完整的基因組獲得以後，從流行於我國山東（ sd ）和黑龍江大慶（ dq ）地區疑似prrs的豬體內分離到prrsv ，在mark - 145細胞上盲傳5 6代，細胞出現明顯病變以後，收獲病毒液，然後提純，提取全病毒rna ，經過反轉錄、 pcr擴增獲得結構基因orf2 7的目的基因片斷，然後與pmd - t載體連接，轉化，得到陽性質粒后進行測序，並將其與ch - 1a株進行了比較分析，同時對這兩個毒株的結構基因組的理化性質進行分析。
  20. The continuing spread of the epidemic and the high rate of infected people in that area of the world have raised the need to establish urgent preventive measures and extend antiretroviral therapy access ( haart )

    在世界上這些地區，這種傳染病的持續性傳播和人群的高感染率迫切要求建立起緊急預防措施和擴展抗逆轉錄病毒的治療方案（ haart ） 。
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