末端蛋白 的英文怎麼說

中文拼音 [mòduāndànbái]
末端蛋白 英文
terminal protein
  • 末 : Ⅰ名詞1 （東西的梢;盡頭） tip; terminal; end 2 （非根本、非重要的事物） nonessentials; minor detai...
  • 端 : Ⅰ名詞1 （東西的頭） end; extremity 2 （事情的開頭） beginning 3 （門類; 方面） item; point 4 （原...
  • 蛋 : 名詞1. （鳥類或龜、蛇類所產的卵） egg 2. （像蛋形的東西） an egg-shaped thing 3. （辱罵之詞）
  • 白 : Ⅰ形容詞1 （似雪的顏色） white 2 （清楚; 明白; 弄明白） clear 3 （空的; 沒加他物的） pure; clear; ...
  • 末端 : end; terminus; terminatio; terminal; tail end; extremity末端棒 terminal bar; 末端朝上 endways
  • 蛋白 : 1. （卵中透明的膠狀物質） egg white; albumen; gary2. [生物化學] （蛋白質） protein
  1. This gland is located on the distal end of spermatophore cyst, and shaped like a semicylinder which consists of many acini

    促雄性腺位於精莢囊末端，半圓柱狀，由許多腺泡組成，細胞內富含粗面內質網和高爾基氏體，推測其分泌蛋白質性質的激素。
  2. J mol biol., 1992, 224 : 53 - 63. 26 abe h, aiba h. differential contributions of two elements of rho - independent terminator to transcription termination and mrna stabilization. biochimie, 1996, 78 : 1035 - 1042

    通過計算，我們預測到266個不依賴終止子，其中包括232個蛋白編碼基因， 12個trna基因和3個rrna基因，約17 %不依賴終止子位於操縱子的末端。
  3. Introduction telomerase is a ribonucleoprotein reverse transcriptase that synthesizes telo - meric dna sequences using its rna as template. it can remedy the loss of te - lomere after cellular mitosis, maintain telomere length and stabilize chromosome

    前言端粒酶（ telomerase ）是一種核糖核蛋白逆轉錄酶，能以自身的rna為模板，從頭合成染色體末端的端粒dna ，彌補細胞分裂時端粒dna的丟失，維持端粒的長度並穩定染色體。
  4. In escherichia coli, arog gene encodes phenylalanine - sensitive 3 - deoxy - d - arabino - heptulosonate - 7 - phosphate synthase isoenzyme arog that catalyzes the first committed step of shikimate pathway. here we study the essential amino acid residues involved in the formation of feedback inhibition site of arog, and the effects of n - terminus on feedback inhibition and its quaternary structure, and the importance of the structural " d2 " symmetry to allosteric inhibition

    本博士論文工作以大腸桿菌k - 12來源的arog為研究對象，通過定點突變、反饋抑制實驗和酶學動力學參數的測定，深入地研究了arog的反饋抑制位點的特性，並對arog的n -末端在反饋抑制機理和維持穩定四級結構中的作用，以及蛋白質結構的「 d2 」對稱性對酶功能的重要性等進行了具體的研究。
  5. The generation of endostatin is catalyzed by proteolytic enzymes, that cleave peptide bonds within the protease - sensitive hinge region of the c - terminal domain

    特異性蛋白水解酶降解膠原c末端的蛋白酶敏感區，產生內皮抑素。
  6. A conservative motif, recognized by proteinases of potato virus y, was inserted between nib and ppiv, which will release functional ppiv from the fused protein after infection by potato virus y. then, plant expression vector pnpa was constructed by ligating the fusing gene and pbi121, which is knocked out gus gene

    以馬鈴薯y病毒的復制酶（ nib ）基因為模板，通過聚合酶鏈式反應獲得nib基因，並在nib基因末端保留了在病毒基因組中nib與外殼蛋白（ cp ）基因相銜接的保守序列。
  7. Telomerase is a ribonucleoprotein complex ( rnp ) composed by its rna component and protein subunits. telomerase can synthesize telomeric dna onto chromosomal ends using its own rna component as a template, elongate the length of telomere, increase cell life and even induce cell immortalization

    端粒酶（ telomerase ）是由端粒酶rna和蛋白質組成的一種核糖核蛋白復合物（ rnp ） 。端粒酶含有引物特異識別位點，能以自身rna為模板，逆轉錄合成端粒dna並加到染色體末端，使端粒延長，從而延長細胞的壽命甚至使其永生化。
  8. The overall structure of the chromosome of s. nanchangensis ns3226was shown to be linear dna molecule with covalently bound terminal proteins. the chromosome telomeres of this strain were seemingly to lie on the two largest chromosomal asei fragments, but the conclusion needs to be refined

    本研究還對南昌鏈黴菌ns3226染色體的結構進行了探索，初步揭示野生型南昌鏈黴菌ns3226的染色體為線性dna分子，末端具有共價結合的末端蛋白，染色體的末端可能處于染色體中最大的兩條ase片段上。
  9. - acetolactate decarboxylase are widely found among bacterial strains but not in other groups of organisms. the enzyme has been demonstrated to be effective for removal of acetolactate and widely used in beer product. in this paper, - acetolactate decarboxylase from bacillus subtilis was purifed to homogeneity from cell extract by ammonium sulfate - fractionation, heat treatment, deae - sepharose fast flow column chromatography

    本文對來源於枯草芽孢桿菌（ bacillussubtilis ） 3226 - 5的-乙酰乳酸脫羧酶經硫酸銨分級沉澱、熱處理、 deae - sepharosefastflow離子交換柱層析等分離純化步驟，得到sds - paeg電泳純，通過n末端氨基酸序列分析驗證酶蛋白的純度。
  10. The protein accumulated mainly in secondary phloem parenchyma cells and secondary phloem ray cells. the degradation of storage protein in terminal branchlets of swietenia macrophylla synchronized with new shoot growth after leaf - absent period, suggesting that the protein was utilized to support the growth of new shoots. when the diminishing of the storage protein below the girdled site was blocked, the new shoot growth was also restrained

    在樹木新的年生長周期中，隨著新梢的發育，積累在末端小枝中的貯藏蛋白質開始被消耗新梢葉片成熟時，末端小枝中的18kda和21kda蛋白質己完全消失，而樹乾和大根中的這兩種蛋白質的含量相對穩定，與落葉期相比幾乎沒有變化。
  11. On the other hand, our previous studies have shown that the nr2b construct with a gfp tag in its n - terminus cotransfected with nr1 subunit can reach the cell surface and be detected by surface staining with anti - gfp antibody in live cells. the nr2b construct will be retained in the endoplasmic reticulum ( er ) when expressed alone in heterologous cells

    我們以往的研究表明，用綠熒光蛋白（ gf內在信號膚下游n末端標記nrzb亞單位，與nri共轉染時能形成與野生型相似的nmda受體通道，且可以通過抗gfp抗體標記活細胞膜表面表達的nmda受體復合物。
  12. Discussion the ends of linear chromosomes are protected by telomeres that consist of double - stranded repetitive sequences complexed with specific telomere - binding proteins

    討論端粒由雙鏈重復序列dna及特異的端粒結合蛋白組成，能保護線性染色體的末端。
  13. As well as in eukaryocyte ( hepg2 and cos - 7 ), then detect their antigenity as a basis study and explore of the choice of immunogen for preventive and therapeutic vaccines of hepatitis b. methods : the gene fragments coding 152aa ( si ) and 124aa ( s2 ) of the carboxyl terminus of hbsag were amplified by pcr from plasmid pecob6 with a pair of primers containing different endonuclease sites and were cloned into multiple cloning sites of plasmid pbks ( + )

    為乙型肝炎的預防和治療性疫苗免疫原的選擇進行初步的研究和探討。方法：本研究利用聚合酶鏈反應（ pcr ） ，通過設計帶有不同酶切位點的一對引物，從質粒pecob6特異性擴增hbsag蛋白羧基末端152個氨基酸（ s1 ）和124個氨基酸（ s2 ）的基因片段，分別將二者克隆到質粒pbks （ + ）的多克隆位點，篩選重組克隆。
  14. To further enhance protein productivity of expression vectors, two artificial transcription activating domains, ah and vp2, were linked to cl represser protein of phage through a soft linker, respectively, and thus two artificial transcription activators were created

    為了進一步提高表達載體表達外源蛋白的能力，我們把兩個人工轉錄激活結構域ah和vp2分別通過一個柔性的linker融合到噬菌體ci蛋白的c末端，構建了兩個人工轉錄激活因子。
  15. The full - length sequence, the 3 ' - deletion fragment, the sequence encoding the mature protein and the sequence encoding the conservative domain, were cloned using synthesized primers. recombinant expression vectors were constructed through directional cloning and then host e. coli were transformed by the vectors

    設計特異引物克隆得到毒蛋白基因的4個片段，即基因全長、末端缺失片段、編碼成熟肽的片段及編碼活性區域的片段。
  16. The former expresses recombinant proteins with a 6xhis tag at n - terminal. the fore mentioned four fragments were all used for expression in this system and the mature protein and the conservative domain were effectively expressed while the expression of the other two was unobvious

    前者表達n ?末端加6 his標記的融合蛋白，克隆到的4個基因片段均進行了表達，其中成熟肽和活性區域得到了大量表達，蛋白全長和末端缺失片段表達不明顯。
  17. The pot1 ( protection of telomeres ) protein binds the singlestranded overhang and is required for both chromosomal end protection and telomere length regulation

    Pot1蛋白與單鏈的突出端結合併被認為是保護染色體末端和調節端粒長度所必需的。
  18. Of seven sweet - taste proteins, brazzein has smallest molecular mass, simply molecular structure and is most heat - stable. in order to make use of brazzein, we have studying on the expression of brazzein gene in e. coli and plants : lettuce and tobacco. the results obtained are summarized below

    為了更好的利用甜蛋白，探討brazzein基因在原核生物和植物中的表達，本論文進行了一些研究，結果如下： 1以合成的brazzein基因為模板，通過引物設計引入突變位點，在基因5 』末端引入ala的密碼子替代原有序列中編碼pglu的密碼子。
  19. Hydrophobicity analysis of the noeb showed that it is a transmembrane protein and includes four transmembrane regions at n - terminal., consisting of three primary helixs and one secondary helix

    疏水性分析發現， noeb是一個跨膜蛋白，在n末端有4個跨膜區，其中包含3個初級螺旋和1個次級螺旋。
  20. However where the product is nonproteinaceous, of low molecular weight and at the end of a long multienzyme sequence it is extremely unlikely that gene transfer to another host will be feasible

    然而，如果產品是低分子量且處于長多酶序列末端的非蛋白質類產品，轉基因技術的應用可行性極小。
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