核蛋白核心 的英文怎麼說
中文拼音 [hédànbáihéxīn]
核蛋白核心
英文
nucleoprotein core-
Lipoprotein lipase ( lpl ) is a critical enzyme of catabolic metabolism in lipoproteins, its major function is the hydrolysis of the core triglycerides of circulating chylomicrons and very low density lipoproteins
脂蛋白脂肪酶是脂蛋白分解代謝的關鍵酶，其主要功能是水解cm和vldl這些脂蛋白中的甘油三酯核心。Cloning and sequence analysis of bos taurus hepatitis c virus core - binding protein 6 homologue gene
牛丙型肝炎病毒核心蛋白結合蛋白6同源基因的克隆化研究Cloning and sequencing analysis of sus scrofa hepatitis c virus core - binding protein 6 homologue gene
豬丙型肝炎病毒核心蛋白結合蛋白6同源基因的克隆化研究Any of the proteinaceous cylindrical hollow structures that are distributed throughout the cytoplasm of eukaryotic cells, providing structural support and assisting in cellular locomotion and transport
蛋白質圓柱形空心結構，廣泛存在於真核細胞的細胞質中，為細胞內的移位和傳輸提供結構支持和協助。Containing many t cell epi - positions and neutralizing antibody epi - positions, the core protein region and envelope protein 2 of hepatitis c virus ( hcv ) structural protein may induce protective immunity responsion in body
丙型肝炎病毒（ hepatitiscvirus ， hcv ）結構蛋白的核心蛋白（ c ）和包膜蛋白2 （ e2 ）含有多個t細胞表位和中和抗體表位，可誘導機體產生保護性免疫應答。Oxygen - evolving psil core complexes treated with hydrophilic crosslinker edc showed a little change in the microenvironments of tyr and trp residues. however, oxygen - evolving psil core complexes treated with hydrophobic crosslinkers such as dcc, hmdi, egs, and dtsp showed a distinctly change in both the microenv
Egs 、 dtsp對psll放氧核心復合物蛋白質中tyr 、 trp微環境和682urn處葉綠素熒光影響大，可能它們參與了psll放氧核心復合物內部的蛋白疏水區域交聯。The full orp encodes a 487 - amino acid protein with a calculated molecule weight of 53. 484 kda and an isoelectric point of 6. 75. at the primary sequence level, it shared high homology with clr, so was named clr - like serine protease, clsp. the clsp sequence has been submitted to genbank / embl ( genbank accession number af178985 )
該蛋白在核酸和氨基酸水平上與人補體組分cl :表現高度同源，故將其命名為補體cl :樣絲氨酸蛋白酶（旦lr一like旦erineprotease ， clsp ） ，該基因已經在ge心ank登錄（登錄號為af17s985 ） 。The pathogenic strains of yersinia enterocolitica carry a 45 - kb high pathogenicity island ( hpi ) comprising iron - uptake - related genes such as irp1 - irp2 and fyua, which has been observed in 93 % of the 60 entero - adhesive e. coli { eaec } strains and 80 % of the e. coli isolated from blood samples
Hpi毒力島功能核心區主要的結構基因為irp2 、 irp1和fyua ，是高度保守的。 irp2和irp1分別編碼兩種高分子量蛋白hmwp2和hmwp1 ， fyua編碼鼠疫菌素受體。At first, 1. 67 u g per well mcab all was coated on three wells of a plate, and then 1. 5 x 1011 phage virion was diluted and added, after incubating with the target, wash away unbound phage by tbst ( 0. 1 % tween - 20 ), the bound phage was eluted with ph 2. 2 tris - gly buffer and amplified, the specially bound phage was enriched by taking through addition binding / amplification cycles. ln the following cycles, the stringency of panning can be increased by raising the concentration of tbst or decreasing that of mcab all, collecting and titering the washing phage of last time and output phage in each round, the selective ratio and the false positive rate of each round were worked out, the gradually increasing of selective ratio and decreasing of positive rate shows that the panning was effective. after 4 rounds of panning, 11 phage clones were selected after competitive - ellsa, the dna samples of 8 positive clones and 1 negative clone were sequenced and all the foreign peptides inserted was also deduced, a clear consensus binding sequence emerged
在本實驗中，利用隨機12肽庫對抗豬瘟病毒（ classicalswinefeverviruscsfv ）糖蛋白me2的單抗a11進行表位篩選，經過四輪篩選以後，隨機挑取11個克隆作競爭- elisa檢測，結果表明，所挑11個克隆中，有9個克隆能對me2蛋白和a11反應產生抑制作用，抑制率最高可達64 ； dna測序以後經過dnastar軟體分析，發現它們的核心序列為anwralsl ，該核心序列與豬瘟病毒e2蛋白的28 - 35位氨基酸ttwkeysh具有同源性；夾心- elisa檢測和western - blotting試驗均證明所挑陽性克隆能被a11所識別；人工合成含核心序列的多肽經間接elisa試驗證實，也能被a11識別。Histologically, diffuse distribution of eosinopholic cardiocytes with pyknosis was noted. immunohistochemical staining for myoglobin discovered wide and diffuse loss of myoglobin throughout the ventricular myocardium. ultrastructurally, the myocardial cell with myoglobin loss were characterized by the presence of swollen mitochondria and packed cellular constituents
組織學檢查注意到彌散性分佈伴有核碎裂的嗜酸性變性，肌紅蛋白組化染色發現整個心室肌廣泛性脫失，超微結構研究表明脫失肌紅蛋白的心肌細胞存在線粒體腫脹和細胞內成分的堆積。It has been known for some time that the acetylation of n - termini of core histones in nucleosome is associated with gene activation
人們很早就注意到，真核細胞中核小體核心組蛋白n -端尾部的乙酰化水平與基因活化密切相關。It is a very basic, single - chain protein with molecular weight about 14 kd. it shares 33 % sequence identity with bovine pancreatic rnasea and has structurally equivalent counterparts for the two histidines and one lysine that comprise the catalytic residues for ribonucleolytic activity
它是由123個氨基酸組成的分子量約為14kd的單鏈堿性蛋白質，與牛胰核糖核酸酶有33的同源性，兩個組氨酸和一個賴氨酸殘基組成了血管生成素核糖核酸酶活性中心。6 feolde e, vigne p, frelin c. angiotensin receptor subtypes and biological responses in the rat heart. j mol cell cardiol, 1993, 25 ( 11 ) : 1359
5田斌，高廣道，曹治平，等.血管緊張素刺激肥大心肌細胞和心肌成纖維細胞核酸蛋白質及膠原合成.中國病理生理雜志， 1995 ， 11 （ 5 ） ： 450By using western - blot, the fusion protein could not be react with antiserum to prrsv, whereas it presented a reactivity with swine antisera against prrsv and mab ge3 by elisa the results implied that the epitope might be one conformational epitope that was mainly composed of aa50 ~ aa55 domain on n protein
Western - blot分析表明表達產物與prrsv陽性血清沒有反應性，而elisa分析表明表達產物可與prrsv陽性血清和單克隆抗體發生反應。由此說明單克隆抗體ge3所識別的抗原表位可能是存在於n蛋白上以kphf為核心的構象型表位。The center is equipped with state - of - the - art facilities, including the most modern two - dimensional gel electrophoresis systems, automatic gel excision and in - gel digestion systems, as well as q - tof and maldi - tof
基因體研究核心設施之一的蛋白體學實驗室，裝備了最尖端的蛋白體By virtue of their different chemical properties, some amino acids are attracted to each other ( for example, oppositely charged amino acids ) and so will associate ; other amino acids will try to avoid water ( because they are greasy ) and so will drive the protein into a compact shape that excludes water from contacting most of the amino acids that " hide " in the core of this compacted protein
由於氨基酸各不相同的化學屬性，有些氨基酸會因為互相吸引（比如電荷相反的氨基酸）會連接在一起；還有些氨基酸因為不親水（因為它們是油性的） ，它們就會驅使蛋白質形成一個緊湊的形狀，以至於不讓水碰到藏在蛋白質核心中的氨基酸。With powerful cells activating function, the product can activate fiber cells in cuticle, assist to produce proteoglycan, obviously remove wrinkles and firm droopy skin, assist to firm cuticle, improve collagen fiber, make skin firm and rich persistently
能強力賦活真皮纖維細胞，幫助核心蛋白聚糖的生成，顯著改善肌膚皺紋、鬆弛現象，有助於真皮的即效回復，快速補充其彈性，增強膠原纖維，持續保持肌膚緊實而富有彈性，製造出充盈緊致的肌膚。Modern biotechnology, represented by gene engineering, cell engineering, enzyme engineering, fermentation engineering and protein engineering, is the forefront for scientific innovation in the 21st century. developing ? iological technique and its relevant industry vigorously has become the core of investment and keystone in economic strategy of many countries around the world. a series of preferential policies and regulations have been set down in order to foster and encourage its development
以基因工程、細胞工程、酶工程、發酵工程和蛋白質工程技術為代表的現代生物技術是21世紀世界科技創新的前沿，大力發展生物技術及其產業已成為各國投資發展的核心產業及經濟戰略重點，並制定了一系列優惠的政策和法規，扶植和鼓勵其發展。The major target of photoinhibition is photosystem ii ( psii ) on which photoinhibition make photosynthetic efficiency decreased, electronic transportation blocked and reaction center protein dl photodamaged
已有研究表明ps是主要靶點，光抑制時表現為： ps光合效率下降、 ps電子傳遞鏈活性下降及核心蛋白被氧化而破壞。In order to screen the precious high protein and the low protein germplasm resources, this experiment determined the grain protein content of 564 wheat core germplasm materials from domestic or foreign countries with near - infrared da7200 method, and screened many precious high protein or low protein germplasm resources
摘要為了篩選高蛋白和低蛋白的種質為資源，以國內外564份小麥核心種質為材料，用da7200近紅外儀測定籽粒蛋白質含量，比較分析了國內外種質資源蛋白質含量的高低，篩選出一批寶貴的高蛋白和低蛋白的種質資源。分享友人