轉錄子 的英文怎麼說

中文拼音 [zhuǎnlùzi]
轉錄子 英文
transcripton
  • 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 （...
  • 子 : 子Ⅰ名詞1 （兒子） son 2 （人的通稱） person 3 （古代特指有學問的男人） ancient title of respect f...
  • 轉錄 : [電學] transcribe; transfer; [聲學] mixing; rerecording; [生物學] transcription; duplicating轉錄...
  1. As a result of haart, hi - infected patients frequently deelop lipid abnormalities, including the accumulation of abdominal adiposity, features of the metabolic syndrome, and other factors that increase cardioascular risk

    作為強化的抗逆轉錄病毒的治療的結果， hi感染的患者經常出現脂類異常，包括腹壁多脂癥的蓄積，代謝綜合癥的特徵和其他的增加心血管危險的因子。
  2. Newcastle disease virus ( ndv ) strain 695, a thermostable nature avirulent strain, were replicated in embryonated chicken eggsand its rna was extracted from allantoic fluid. referred to the reported sequence of f gene, a pair of primers were designed and synthesized. f gene of ndv b95 strain was amplified by rt - pcr, the pcr products were checked by agrose gel electrophoresis and purified by agrose gel fracion method

    利用從國外引進的新城疫熱穩定性天然弱毒b _ （ 95 ）株接種spf雞胚繁殖病毒，經處理后提取病毒的基因組rna ，參考國內外發表的ndv融合蛋白基因序列，設計一對特異性引物，經反轉錄聚合酶鏈式反應（ rt - pcr ）擴增出約1700bp大小的特異性片段，將此片段回收純化后，利用t - a克隆技術將其克隆到pgem - t - easy克隆載體中，再轉化大腸桿菌jm109感受態細胞，轉化后經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。
  3. Comprehensive cellular responses was found in human amnion fl cells following exposure to low concentration of mnng, such as the lowering of dna replication fidelity resulted from alteration of dna polymerase profile ; activation of a lot of transcription factors, such as api, creb, nf - kb etc ; clustering of egfr ( epidermal growth factor receptor ) and tnfr ( tumor necrosis factor receptor ) and activation of camp - pka - creb and jnk / sapk signal pathways

    我們發現，低劑量mnng處理后的人羊膜fl細胞有廣泛的細胞反應，並有多個信號轉導通路的激活和基因表達的改變。例如dna復制保真度下降， dna聚合酶譜發生改變，應用報告基因技術和底物磷酸化檢出技術證明細胞一系列轉錄因子如ap1 、 creb 、 nf b等被激活，細胞表面受體如表皮生長因子受體、腫瘤壞死因子受體發生聚簇，細胞信號轉導通路camp - pka - creb和jnk sapk被激活。
  4. At rest, the heterodimeric rel / nf - k b complex is located in the cytoplasm bound to an inhibitory factor, i k b. upon stimulation, i k b is phosphorylated and degraded, free nf - k b then translocates into the nucleus where it binds to k b site to regulate transcription

    靜息時， re皿4bh聚體與抑制蛋白kbs結合，在細胞漿中保持無活性。受到刺激， ikb分子迅速磷酸化並降解，釋放nf兒b轉位入核，通過與kb位點結合調節轉錄。
  5. It refers to the release of the viral genome from its protective capsid to enable the nucleic acid to be transported within the cell and transcribed to form new progeny virions

    它指的是將病毒基因組從它的保護性衣殼中釋放出來，使核酸能在細胞內轉運並能轉錄以形成新的子代病毒。
  6. But without rdrp transcription were tested. so it is suggested that tm - 22 is a relative to multi - protein transcriptional coactivator. mip204 and pr - la gene expression can be induced in resistant response and do not relate to rdrp gene transcription

    因此，可以認為tm一22基因的編碼蛋白與復合蛋白轉錄因子有關，在抗病反應中能夠誘導五刃滬204和屍尺一ia基因的表達，與rdrp基因的轉錄沒有直接的聯系。
  7. 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。
  8. The regulating roles of transcription factors in embryonic erythropoiesis

    胚胎期紅系造血中轉錄因子的調控作用
  9. Advances in retrotransposon in animal genome

    動物基因組中反轉錄轉座子的研究進展
  10. Dreb - type transcription factors can accept stress signals from environment and promote the expression of stress - tolerant genes. four dreb homolog genes, gmdreba, gmdrebb, gmdrebc and osdreb4 - 2 were isolated from soybean [ glycine max ( l. ) merr. ]

    Dreb類轉錄因子能接受逆境信號並啟動逆境應答基因的表達。在本研究中，以大豆和水稻為材料，共克隆了4個dreb的同源基因，分別命名為gmdreba ， gmdrebb ， gmdrebc和osdreb4 - 2 。
  11. 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 。
  12. 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。
  13. The tumor cells transfected with restin are arrested in gl phase and the cell proliferation is inhibited. it implies that restin may be correlated to cell cycle regulation. other data showed that the necdin, a homolog of restin, could suppress cell growth by interacting with transcription factor e2f1 and p53

    而與restin的同源蛋白的necdin ，可以與細胞周期促進蛋白sv40大t抗原、腺病毒eia 、轉錄因子ezfi等相互作用，抑制細胞生長;也可以和轉錄因子p53作用參與生長抑制和抑制p53誘導的細胞凋亡。
  14. Considering alcaligenes faecalis pencillin g acylase ( afpga ), which possesses the attractive characteristics for beta - lactam antibiotics conversions, the gene of pga was cloned into two expressing vector pkkfpga and psmlfpga. both the constructed plasmids psmlfpga and pkkfpga contained the pga gene, trc promoter and rrnb transcript terminator, differ in the replicon and antibotic marker, pkkfpga contained multicopy replicon ( cole 1 ) and ampicillin marker. while psmlfpga contained medium - copy replicon ( p15a ) and tetracycline marker

    本文將糞產堿桿菌青霉素g酰化酶（ afpga ）基因構建表達載體pkkfpga和psmlfpga ， pkkfpga和psmlfpga均含trc啟動子、青霉素g酰化酶基因、 rrnb轉錄終止子，其中pkkfpga含有氨卞青霉素抗性基因和cole1高拷貝復制子；而psmlfpga含有四環素抗性基因和p15a中拷貝復制子。
  15. This experiment passing to grope for the carbon source constitutes of the culture medium and using t. reesei rut c - 30 induced the expression of # - mannanase ( # - 1, 4 - mannan mannohydrolase ec 3. 2. 1. 78 ). in this experiment i put the constant carbon source ( lactose and locust bean gum ) in the foundation culture medium ( mandels nourishment liquid ) of t. reesei rut c - 30, then proceeded the variable carbon source ( dragon spruce fiber, com rush pith fiber, wheat straw fiber, wheat straw xylan, corn rush pith xylan, dragon spruce mannan ) to single factor, double factor, three factor, four factor and five factor orthogonal experiment. 1 determined the activity of p - mannanase using locost bean gum as substract by the 3, 5 - dinitosalicylic acid method, and observed the growing situation of the gernic at the end i selected the directions for the inducement expression of the # ? mannanase from trichoderma reesei rut - c30 that contained the dragon spruce fiber, wheat straw xylan, dragon spruce mannan

    在里氏木霉rutc - 30的基礎培養基（ mandels營養液）中加入固定碳源乳糖和槐豆膠，然後將可變碳源（雲杉纖維、玉米芯纖維、麥桿纖維、麥桿木聚糖、玉米芯木聚糖、雲杉甘露聚糖）進行單因子、雙因子、三因子、四因子、五因子的里氏木霉rutc - 30正交培養實驗，並以槐豆膠為底物用3 ， 5二硝基水楊酸法測定培養液中?甘露聚糖酶的活力。從而確定了酶活最高且菌體生長良好的含雲杉纖維、麥桿木聚糖和雲杉甘露聚糖的誘導培養基為最佳培養基，用該培養基培養的里氏木霉（ t . reesei ） rutc - 30使其轉錄的-甘露聚糖酶（ - 1 ， 4 - mannanmannohydrolaseec3 . 2 . 1 . 78 ） mrna量能夠滿足rt - pcr的要求。
  16. 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。
  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. Northern blotting indicates that wnk1 is widely expressed in different tissues and has two transcripts, whereas wnk4 is expressed primarily in kidney

    Northern印跡雜交表明wnk1廣泛表達在人類、大鼠和小鼠的各個組織中，有兩個轉錄子。而wnk4則主要在腎臟中表達。
  19. His research focuses on the molecular mechanics of pre - mrna splicing, the evolution and regulation of alternative splicing, and splicing defects associated with cancers and inherited diseases

    他的研究集中在轉錄子剪接的分子機制、選擇性剪接的演化和調節，以及和剪接缺陷有關的癌癥及遺傳疾病。
  20. 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。
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