組成型表達 的英文怎麼說

中文拼音 [zǔchéngxíngbiǎodá]
組成型表達 英文
constitutive expression
  • 組 : Ⅰ名詞1 （由不多的人員組成的單位） group 2 （姓氏） a surname Ⅱ動詞（組織） organize; form Ⅲ量詞（...
  • 成 : Ⅰ動詞1 （完成; 成功） accomplish; succeed 2 （成為; 變為） become; turn into 3 （成全） help comp...
  • 表 : Ⅰ名詞1 （外面;外表） outside; surface; external 2 （中表親戚） the relationship between the child...
  • 達 : Ⅰ動詞1 （暢通） extend 2 （達到） reach; attain; amount to 3 （通曉; 明白） understand thoroughly...
  • 表達 : deliver; express; show; voice; convey; communicate
  1. Deduced amino acid sequence of s1, s2, pvin were also highly homologous each other ( 98 %, 99 % in each case ). the stilbene synthase genes were excised from the plasmids by bamh i and sac i digestion and intergrated into a binary vector, pbi121 and pev2, from which the p - glucuronidase ( gus ) gene sequence had been removed by the same digestion to prepare a 35s promoter - stilbene synthase 2 - nopaline synthase polyadenylation site construct and a tfp2 promoter - stilbene synthase 1 - nopaline synthase polyadenylation site construct. the recombinant plasmids were called pbs2, pev2s 1. respectively

    用bamhi和saci同時酶切ps2 （ s2表示來自雷司令的芪合酶基因） 、 ps1 （ s1表示來自粉紅玫瑰的芪合酶基因）以及pbi121 、 pev2 ，使得s2 、 s1分別插入替代pbi121 、 pev2中的gus基因，構建成植物表達載體pbs2 、 pev2s1 ， pbs2中含camv35s組成型啟動子，使s2基因能在番茄植株的各個部位表達； pev2s1則含有果實特異性啟動子tfp2 ，使s1基因只在番茄果實中表達。
  2. The deleted mutant pap gene was also cloned into yeast secreted expression ppic9k vector to form ppic9k ~ 3, then the vector was transferred into pachia pastoris gs115 strain. the specific expression protein was secreted into the medium after inducing with methanol and the protein amount reached about 50 - 60 u g per millilitre measured by uv - absorbed methods in the supernatant of the medium via high density fermentation. sds - page results showed that there was one protein band in the gel which molecular weight was about 34ku

    將缺失型pap基因克隆于酵母分泌型表達載體ppicgk構成重組載體，然後導入畢赤酵母（ p8chianastoris ）菌株gslls細胞中，在甲醇的誘導下，經過酵母高密度發酵進行pap的表達，經sds page分析，結果表明，在培養基上清液中含有一明顯的特異性蛋臼條帶，大小為34ku ，經western blotting分析，該蛋白與法國pap抗血清有特異性反應，體外活性檢測表明該蛋白對tmv的侵染性具有高度的抑制性，說明該pap基因在畢赤酵母gs中也得到了正確表達。
  3. These results indicated that the cloned osg6b " had a constitutive characteristics but not anther specificity, and the transgene was segregated in a mendelian fashion in the tl generation

    研究表明，所克隆的osg6b 』不具有花藥特異性，而具有組成型表達的特徵。第二部分：從大腸桿菌e
  4. This gene, artificially put under the control of camv 35s, was introduced into tobacco with the aid of agrobacterium, and the transgenic plants obtained were identified by gus staining, pcr and southern blot analysis

    將arge與組成型啟動子camv35s相連，構建植物表達載體，通過農桿菌介導轉化煙草。經過gus染色、 pcr及southern鑒定獲得了轉基因植株。
  5. Driven by the cauliflower mosaic virus ( camv ) 35s promoter, the er - shsp over - expressed constitutively. the growth and the phenotype of transgenic plants can be used for researching the function of er - shsp in improving tomato ' s cold resistance and the er - shsp chaperones function in vivo. after degested by kpnl and xbal enzymes from the pbs - er plasmid, the gene er - shsp - lehsp21. 3 was inserted into the prokii vector to construct an eukaryotic expressing vector

    利用基因工程方法，將內質網小分子熱激蛋白基因（ endoplasmicreticulum - locatedsmallheatshockproteingene ， er - shspgene ） - lehsp21 . 3導入到番茄體內，使之在植物體中組成性表達（ constitutiveexpression ）內質網小分子熱激蛋白（ er - shsp ） ，觀察轉基因番茄在低溫條件下的生長和表型反映，研究er - shsp在提高植物耐寒性中的作用，同時為體內研究er - shsp的分子伴侶機制提供依據。
  6. By changing pichia pastoris ' s metabolic path rationally, a constitutive recombinant p. pastoris sibas 5071 with riched sam synthetase was obtained on the basis of research of sulfide ' s metabolism in yeast in our laboratory

    本實驗室在對酵母細胞中含硫物質代謝研究的基礎上，通過合理改造pichiapastoris的代謝通路，獲得了一株組成型表達sam合成酶2 （ sams2 ）的重組p . pastoris菌株sibas5071 。
  7. As both the recombinant plasmids and the host dh5a had no laciq gene which encode lac represser, the trc promoter was not repressed by lac represser and always active. therefore the afpga could be constitutively expressed without iptg induction in the host dh5. in the shaking flask, the optimum ph and temperature for afpga expression was 7. 0 and 30

    兩重組質粒再轉化宿主菌dh5 ，由於重組質粒和宿主菌dh5均不含laci ~ q調控基因，重組菌不產生阻遏蛋白，控製表達的trc啟動子始終處于「開」狀態，因而所得重組菌dh5 pkkfpga和dh5 psmlfpga不需誘導便能組成型表達pga 。
  8. The author first proposes an improved mass - spring model developed for rectangle meshes based on the survey of cloth modeling methods, by which the simulation of cloth is formulated unifiedly. the dynamic system of modeling and simulation is derived and solved using time differentiate method, with given composition and expression of internal and external cloth forces in the formulation

    在此基礎上作者提出改進的基於矩形域的質點-彈簧模型，利用該模型統一建立了布料真實感模擬方程，給出方程中質點所受內力和外力的組成與表達式以及動態系統的推導和求解過程，並且描述了模擬的具體實現演算法。
  9. In this dissertation, influences of various factors on plant regeneration and agrobacterium - mediated transformation of tall fescue embryogenic calli were systematically studied, and thereafter, stress tolerance - related cbf1 gene guided by constituent promoter camv 35s was incorporated into genome of this grass to obtain transgenic plants with increased stress tolerances

    本論文在對高羊茅胚性愈傷組織植株再生與農桿菌介導遺傳轉化的多種影響因素進行系統研究的基礎上，將組成型表達啟動子camv35s引導的耐逆相關cbf1基因導入該草種的基因組，獲得耐逆性增強的轉基因植株。
  10. The class ii transactivator ( ciita ) expression appears to be an absolute requisite for expression of class ii mhc, whether constitutive or inducible

    無論是組成型還是誘導型類分子表達， mhc類分子轉錄活化因子（ c ta ）都是絕對必需的。
  11. Constitutive expression of class ii mhc is restricted to " professional " antigen - presenting cells but can be induced on various tissues by gamma interferon

    Mhc -類的組成型表達僅限於「專職性」抗原提呈細胞，但細胞因子如ifn -可引起誘導型類分子表達。
  12. Analysis of acbadh expression in leaves showed that the expression levels of acbadh increased about 10 - fold after plants were treated with nacl and aba for 48 hours when compared to control plants respectively

    Northernblotting雜交結果表明， badh具有組成型表達的特性。 100umaba和400mmnacl處理48小時后， badh的表達增加10倍左右。
  13. A fusion - trascriptional library was then constructed by inserting sau3ai - partially digested chromosomal dna from 7653r into bamhi cloning site of phn127. a group of constitutive - expression fusions with different fluorescent strength were obtained

    將7653r的總dna經sau3ai部分酶解並克隆到phn127上，獲得的融合子庫，從中篩選到gfp組成型表達的具有調控活性的dna片段。
  14. However, so far only the results obtained by whitelaw et al ( 2002 ) concerning leetrl gene were partly consistent with the negative model and partly against it. obviously, the action models for these ethylene receptors are far from being clearly understood

    目前已經從模式植物番茄中分離了6個受體基因（ leetr1 6 ） ，對它們的基因和蛋白結構特徵、表達特性等已經有較多的研究，但是對組成型表達受體基因在乙烯受體系統中的功能研究較少。
  15. The promoter - probe vector phn117 in e. coli and phn127 in g " were further constructed by removing promoter while keeping sd sequence from phn115. a teta / tetr bidirectional promoter fragment from pbr322 was respectively cloned into phn117 and phn127 and the resulted colonies were all fluorescent

    並經插入pbr322上665bpteta tetr雙向啟動子片段后得到的轉化子均發綠色熒光驗證，實現了wtgfp在大腸桿菌和華癸中生根瘤菌中的組成型表達。
  16. Third, we examined the expression of ecbp21 dynamics during the incubation of angelica suspension - cultured cells and stress treatments through northern blot analysis. during the incubation of angelica suspension - cultured cells, the expression of ecbp21 gene increased from 0 to 12th day, and it reached a peak on the twelfth day. while the expression of cam gene increased from 0 to 9th day, and it reached a peak during the 6th - 9th day

    3 . ecbp21表達分析: northernblot分析表明:在白芷懸浮培養細胞生長周期中， ecbp21和cam都為組成型表達， 0一12天ecbp21表達量逐漸增加，第12天達到最高，隨后12一21天， ecbp21表達量稍有下降，維持在一個比較穩定狀態;而o一6天時， cam表達量逐漸上升，第6一9天達到最大表達量，隨后， 9一21天， cam表達量有所下降。
  17. The plant expression vector pbin19 - rok219 was constructed, which contains cauliflower mosaic virus ( camv ) 35s promoter and noster. introduction of ibdv vp2 gene under control of camv 35s promoter resulted in the construction of binary expression vector pbr - vp2. then the vp2 gene was in the left and right border regions, which denote the limits of the dna that is integrated into the plant genomic dna via agrobacterium fwme / ac / ms - mediated transformation

    構建了表達載體pbin19 - rok219 ，以ibdv甘肅天水株的抗原基因vp2為目的基因，將vp2基因置於植物組成型表達啟動子camv35s之下，構建了一個ibdvvp2基因的植物表達載體pbr - vp2 ，這樣使vp2基因位於農桿菌t - dna的左右邊界重復序列之間。
  18. We have created transgenic tobacco plants in which expression of the atnced3 coding region is under strong constitutive 35s cauliflower mosaic virus ( 35s ) promoter, stress - inducible rd29a promoter or stomotal - specific kst1 promoter by agrobacterium tumefaciens - mediated transformation

    構建了組成型35s 、誘導型rd29a 、氣孔特異表達性kst1啟動子驅動atnced _ 3基因表達的真核表達載體，通過農桿菌介導的葉盤法轉化煙草，得到了轉基因植株。
  19. In one of the cases, the positive rate of cd25 was decreased by 17. 1 % meanwhile mean fluorescent intensity by 50. 8 %, also the positive rate of cd69 was decreased by 16. 7 % meanwhile mean fluorescent intensity by 56. 7 %

    7 ，平均熒光強度降低56 7 。上述結果表明：反義c11ta可以部分抑制組成型和誘導型mhc刁類分于的表達，導致t細胞活化受到影響。
  20. It sets up the improved spring - mass model, derives the formulation for dynamic system of modeling and simulation with given composition and expression in internal and external cloth forces, describes the simulation algorithm

    摘要對彈簧質點模型進行了改進，給出模型方程中質點所受內力和外力的組成與表達式以及動態系統的推導和求解過程，並且描述了模擬柔性受風飄動的具體實現演算法。
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