細目篩 的英文怎麼說

中文拼音 [xìmùshāi]
細目篩 英文
micro mesh sieve
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 目 : Ⅰ名詞1 （眼睛） eye 2 （大項中再分的小項） item 3 [生物學] （把同一綱的生物按彼此相似的特徵分為幾...
  • 篩 : 名詞[書面語] （植物名） sedge
  • 細目 : 1. （詳細的目錄） detailed catalogue2. （詳細的項目） specific item; detail; enumeration
  1. The other method is to pass the powder through 200 or fine mesh screen.

    另一種是把軟木粉用200目或更細的篩網進行篩選。
  2. For the purpose of exploiting the affluent resource of traditional chinese medicines, rat pheochromocytoma pc 12 cells were used as a model to screen the neuroactive components from natural products. most of all, the effect of it on inducing the differentiation of pc 12 cells and / or execute the neuroprotective effect challenged by serum - deprivation and oxidative pressure, and its mechanism were studied in this paper

    本文以利用我國豐富的天然藥物資源為目的，用大鼠嗜鉻神經瘤細胞pc12作為模型，篩選能模擬ngf的功能誘導pc12細胞分化、對神經細胞有一定保護作用的天然藥物，並對其作用機制進行初步探索。
  3. According to above consideration, experiments was carried out as below : first, targeted gene - human serum albumin ( hsa ) gene was obtained via pcr technology. secondly, the hsa gene was liganded with a plasmidprla22 whose two arms carry dna sequences necessary for crossing with the human a - lactalbumin yac to form an integration vector prla - hsa, then the integration vector plasmid was co - transformated into the right yac - bearing yeast with another plasmid plrh33 which carrys a selective gene

    因此，本試驗首先擴增出整合在酵母基因組里的人血清白蛋白（ hsa ）基因作為目的基因，並將人血清白蛋白基因插入到一個含有人-乳白蛋白yac同源序列的重組型質粒載體，以構建整合型載體，再與另一個帶篩選基因的質粒共轉化入含人-乳白蛋白yac的酵母細胞體內。
  4. Fine screens have openings of 3/16 inches or smaller.

    細格篩的孔目為316英寸或更小些。
  5. Fine screens have openings of 316 inches or smaller

    細格篩的孔目為3 16英寸或更小些。
  6. Fine screens have openings of 3 / 16 inches or smaller

    細格篩的孔目為3 16英寸或更小些。
  7. The wenshin rotary frames the process is rigorous, after all members pass through counsels committee member strict verification screening are accepted, also once turned down the public figure who some have not been able to tally hold a round basic idea, the essence has selected chooses the heavy tar not weight thin, although at present only then 32 people actually each one are “ the elite ”, guarantees exchange if not genuine “ the rotarian ”, is not studies has the being expert in scholar, professor, is the enterprise has the studying enterprise outstanding person

    文心社社員的羅織過程是嚴謹的，所有成員均經輔導委員嚴密的審核篩選后入圍，也曾婉拒了一些未能符合扶輪基本理念的人士，精挑細選重質不重量，目前雖然只有32人卻個個是紅心，如假包換的扶輪人，不是學有專精的學者、教授，就是事業有專攻的企業精英。
  8. Multicopy integrants were screened with g418 from pichia pastoris which contains recombinant plasmid, and induced with methanol to secrete interesting peptide. the supernate of pichia pastoris culture was analysed by sds - page and western blotting. a reactive band, which the apparent molecular weight is 36kd, can be detected with sheep anti - hcmv polyclonal antibodies

    重組質粒轉化巴氏畢赤酵母， g418篩選出多拷貝插入的單克隆，甲醇誘導多拷貝插入的單克隆酵母細胞分泌目的蛋白，培養液上清經sds - page電泳分析，在蛋白質印跡中檢測到培養液上清有一表觀分子量為36kd ，能與羊抗hcmv多克隆抗體發生發應的條帶。
  9. But no screening test can currently reveal which eggs have done the best job of reprogramming adult cells - although several research groups are working to develop such a test for agricultural use

    但目前篩選實驗還不能顯示哪些卵子在對成熟細胞重新編程時做得最為出色雖然幾個研究小組正在進行這類實驗以便在農業上應用。
  10. The interesting gene fragment with ecori and noti were amplified by overlapping pcr, which inserted into vector plasmid ppic9k after degisted by ecori and noti, and the recombinant plasmid was transformed into competent dh5cc. positive clones were screened by pcr from the lb plate with amp. digesting analysis resulte shows that the interesting gene were inserted into the vector ppic9k with correct direction

    目的基因經雙酶切后連接載體ppic9k ，然後導入大腸桿菌dh5中，在含氨卞青霉素（ amp ）的lb板上用pcr反應篩選出陽性菌落，雙酶切結果表明目的基因已插入載體中，且方向正確，測序結果進一步證明人巨細胞病毒重組基因表達質粒成功地克隆了目的基因片段。
  11. Then the amplified mtb8. 4 and ms gene were subcloned into the unique nhe i and mlu i cloning sites of pci - neo expression vector

    重組質粒pm 、 pms轉染ps15細胞，進行穩定表達， g418篩選抗性克隆后，用rl 』 - pcr檢測目的基因在mrna水平的表達。
  12. Expression in vitro cos - 7 cells were transfected with pm, pms, pmi and pmsi constructs by cationic liposom, respectively. 48 hours later, mrna of targets gene were detected by rt - pcr and hil - 12 protein in culture supernatnant and cell lysates were detected by western blotting. p815 cells were transfected with pm and pms constructs and selected by g418

    2 .重組質粒在真核細胞中的表達: （ 1 ） pm 、 pms轉染cos一7細胞， 48小時后，用ri 』 - pcr檢測目的基因在mrna水平的表達;轉染p815細胞， g418篩選抗性細胞克隆，用rt - pcr檢測目的基因在mrna水平的表達，結果為陽性，說明在轉錄水平有目的基因的表達。
  13. The recombinant fasl - ecd was purified and its biological activity was analyzed on several cell lines and the most sensitive cell lines are selected. ( 2 ) using a computer program, a single short peptide is derived from antisense homology box of fas ligand and is chemically synthesized. ( 3 ) examine the apoptosis - inducing effect of the recombinant fasl - ecd and the ten - peptide on the most sensitive cell lines, and the relationship between them was analysed

    純化重組蛋白fasl - ecd ，並分析其生物學活性，篩選出對之最敏感的腫瘤細胞株； （ 2 ）根據生物信息學軟體分析結果，選取fasl胞外區256 - 265的十肽（ n ） - hlyvnvsels - （ c ）作為目標分子，委託生物公司合成該十肽； （ 3 ）分析fasl - ecd和十肽對最敏感腫瘤細胞的毒性作用，分析重組fasl一ecd及十膚作用的相關性。
  14. We obtained our transgenic material, the rice suspension cells, by inducing embryonic rice callus. then we constructed the expression vector pca - ced9, and transferred ced - 9 gene into the rice callus and embryogenic suspension cells. the work of using hygromycin selective medium to obtain regenerated plants is still going

    構建了用於水稻中表達的載體pca - ced9 ，通過農桿菌eha105轉化導入水稻愈傷組織和水稻懸浮細胞，經潮黴素（ hym ）篩選，以期望獲得抗性植株，目前該工作仍在進行中。
  15. The common inducing protocols, including specific inducers, five - step induction, stromal cell coculture and gene transfection, are not very effective, with the shortcomings of complicated manipulation and high costs

    目前常用誘導方法包括使用特異性誘導劑、 「五步誘導法」 ，還有尚有爭議的基質細胞共培養法，以及基因轉染與篩選，但有操作復雜、費用高、毒性大等缺點。
  16. In view of the research situation of the technologic and economic evaluation on the constructed program of the pacific road " section in the no : 1 route of wuhan city ' s light rail transit at present, especially the researchment on the trend of the route, the paper discussed detail research of the constructing plans by using various theories of fundamental construction econnmics, etc, based on the the general urban constructing plan of wuhan, etc. the qualitative analysis method and the quantitative analysis method are connected to be applied into this paper for the research work

    本文根據《武漢市城市總體規劃》 （ 1996 - 2020 ） ， 《城市快速軌道交通工程項目建設標準》 ， 《武漢市綜合交通規劃》 （ 1996 - 2020 ）以及運籌學、技術經濟學、投資管理學、基本建設經濟學等原理和相關理論，對武漢輕軌交通一號線太平洋路段這部分關鍵建設線路方案的比選進行了論述及細化研究。本文採用定性分析與定量分析相結合的方法，對軌道線網初始方案進行測試與調整；對多個線路走向的初始方案進行篩選，確定兩個備選方案，再對軌道交通線網優選方案進行綜合比選評價，最終得出軌道交通線網的推薦方案，增強了建設方案的科學性和合理性。
  17. The results given by the improved software are not both statistically and biologically different from manually specified results, and thus can be used as an effective alternative for the latter. it has a very high sensitivity in determining cells with a tail, meeting the needs of screening tests. it has both a high sensitivity and a high specificity in determining cells with 2 damage grade, indicating a potentially good laboratory index

    結論彗星試驗圖像分析軟體經改進后，分析準確性得到提高，程序魯棒性增強，而且易用性改善，並增加了由操作者進行必要校正的功能;所得分析結果與人為指定的分析結果相比，並不同時存在統計學顯著差異和生物學顯著差異，可作為真實可靠的彗星數據分析系統應用;改進后的系統在拖尾細胞判定上具有很高靈敏度，可用於篩查試驗項目;在2級及2級以上損傷細胞的判定上同時具有較高的靈敏度和特異度，是實驗室研究中的優良指標。
  18. In order to establish an intelligent screening system of tax assessment, this article studies the data mining technology and explains its application in tax assessment

    本文以構建基於數據挖掘技術的納稅評估對象智能篩選為目標，通過對數據挖掘技術的學習研究，詳細闡述了數據挖掘技術在納稅評估指標生成中的應用。
  19. Major difference of hn proteins lies in no. 18 - no. 75 amino acid residues on n - terminal which includes three active sites of hn protein. the influence on biological action, caused by the difference of hn protein, is needed to study further. hn gene has only four glycosylation sites, which is 1 or 2 less on amount than that of other strains. so, this difference can be take on as a natural mark of ndv b95 strain furthermore, the fragment encoding hn gene was excised from the positive clone pgem - hn with sail and saci enzyme, and purified by agrose gel fraction method. then the fragment was subcloned into the pet - 28c expressing vector digested by sail and saci restriction enzyme

    作者將正確的重組克隆質粒pgem - hn用saii 、 saci雙酶切，電泳回收目的片段，將其亞克隆到經saii 、 saci雙酶切處理的pet - 28c中，轉化大腸桿菌tgi感受態細胞，得到的轉化子經pcr鑒定和酶切分析，篩選出符合閱讀框的重組子，構建成重組表達質粒pet - hn ，並在大腸桿菌bl _ （ 21 ） （ de _ 3 ）宿主菌中成功地表達了含目的蛋白的融合蛋白，融合蛋白的分子量約66kd ，加入iptg誘導8h后，蛋白表達幾乎達到最高水平。
  20. Plenty of contrast experiments have confirmed previous research conclusion is rightly. firstly according to the principle of reasonable grading, product has better performance when quartz sand mill to the 200 eye 0. 6 % and tailings mill to the 200 eye 1. 4 %

    經過大量的對比實驗，證實了早先研究結論的正確，根據合理級配的原理確定出在石英砂細磨至200目篩餘0 . 6 、尾礦粗磨至200目篩餘1 . 4的條件下，製品具有較好的性能。
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