u-g 中文意思是什麼

u-g 解釋

  • u : （pl U s u s ）1 英文字母表第二十一字母。2 U 字形的東西。3 〈U〉 鈾的符號（＝ uranium）。 U bolt ...
  • g : 1. generator. 2. German. 3. Germany. 4. giga 十億。5. Gossypium 棉屬。6. grid. 7. Gulf. 8. 【軍事】 gun.
  1. It contains more then 4, 000 chemicals which includes poisons and carcinogens. e. g. tar, nitcoine, carbon monoxide, ammonia, dimethylnitrosamine, formaldehyde, hydrogen cyanide and acrolein. the u. s. environment protection agency has classified secondhand smoke as a group a carcinogen

    二手煙霧含有4 ， 000多種的化學粒子和氣體，當中還包括了焦油、尼古丁、苯並芘等粒子，以及有毒氣體如一氧化碳、亞摩尼亞、甲醛、丙烯醛等。
  2. Methods : hepatocytes obtained from mice with in situ portal vein collagenase perfusion were inoculated on two types of medium, which one was 10 % pcs rpmi 1640 medium ( common medium ), the other was rpmi 1640 medium supplemented with 5 u g / ml tranferrin, 5 u g / ml insulin, 10nm nicotinamide, 5mm - me, 40 u g / ml hgf ( special medium )

    一種是在rpmi1640培養液中加入了511iml轉鐵蛋白、 5pg ml牛胰島素、 10nm煙酚胺、 smm卜琉基乙醇， 4011g ml促肝細胞生長因子，簡稱為肝細胞培養液。
  3. 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。
  4. The reasults are summed up as following : ( 1 ) the more metaphase chromosomes of bmn cells and moderately contraction can be obtained by air - drying after cultured at the colchicine concentration 1. 0 u g / ml, 28 " c, for 6 - 9h

    用空氣乾燥法和培養細胞貼片法對bmn細胞的染色體和有絲分裂進行研究發現： （ 1 ）採用空氣乾燥法制備bmn細胞的染色體，在終濃度0 . 1ug / ml的秋水仙素28培養6 9h條件下可得到較多中期分裂相，染色體的凝集也比較適中。
  5. Then were electrophored. the extent of dna migration were measured. index - percentage of " comet " cell and " comet tail " were analysed that indicated when vero cells were treated with 2 u g / ml quinocetone vero cells got midium - grade damage, and were treated with 6 u g / ml olaquindox vero cells got midium - grade damage

    喹乙醇染毒劑量在2 10 g ml時細胞存活率90 ，以2 10 g ml劑量的喹乙醇染毒處于對數生長期的vero細胞，后經過電泳，通過分析彗星樣細胞發生率和彗尾長短等指標，結果表明染毒劑量在6 g ml對dna造成中度損傷。
  6. 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。
  7. The finding of dnaase in the earthworm the tissue extract of earthworm which had been diluted 28 times could digest 4 ul pbv220 - r - inf ( 6. 66 u g / ul ) completely at 37 @ in a hour but it had no effect on rna

    雙胸蚓組織中dna酶的發現28倍稀釋雙胸蚓組織粗提液37保溫1小時，可將4vlpbv220 。 y一inf質粒（ 6石6119 11l ）完全消化但對rna無消化作用。
  8. No trace of any newly expressed protein band was noticed in supernant as well as in the cells by sds - page, except the verification of the substitution of beta - galactosidase gene ( the lose of galactosidase protein band ), which is a selective marker of the wild - type virus. elisa test results suggested the expression of egf in cells, but not in culture supernant. the quantitative calculation suggested the expressed egf was about 6 - 7 u g ( as egf standard ) per flask ( 2 > < 106 cells ) in the cellular extract

    將重組病毒rbmbacph - egf以10moi感染bmn細胞， 72小時后收集培養細胞和上清；培養上清和經超聲波處理的細胞樣品elisa檢測發現胞內樣品中存在能與egf抗體免疫反應的產物，粗略估計表達量約6 7 g 2 10 ~ 6個細胞（相當于egf標準品） ；重組病毒rbmbacph - egf穿刺接種5齡家蠶幼蟲，每隔24h收集蠶血淋巴，經elisa檢測發現第4天表達量最高，根據egf標準曲線計算蠶血淋巴的表達量約32 g ml ； elisa定性實驗還發現正常蠶血也存在與egf抗體間交叉反應的物質。
  9. 4. da release from amy of female and ovx rats increased as early as 5min after i. c. v injection of effective contraction of wujibaifengwan at doses of 300 u g / ml, 600 u g / ml 2. 5 u 1 respectively and returned to the level of control rats within 40min

    側腦室分別注射烏雞白鳳丸有效成分300pg hl ， 600119 hl2 5nl ，均能迅速增加內）雌鼠和ovx鼠電刺激誘發的amyda釋放量，增高時間約40min ，並表現出一定的量效關系。
  10. L ) the existence of local solutions in the part of the existence of local solutions, we investigate the intial boundary value problems for the more general quasilinear system : we consider the existence of local solutions of the system ( 2 ) when it may be a cross - diffusion system and u g ( g is a open subset of rn ). in order to use the results of h. amann [ 1 ] on local existence for quasilinear systems ( 2 ), we find that the results of h. amann on the corresponding linear system were not proved completely. especially for the case of cross - diffusion systems ( 2 )

    1 ）局部解存在性在局部解存在性部分，我們研究的為更一般的擬線性耦合方程組的初邊值問題：我們研究了在u g （ g是使散度型方程組（ 2 ）中的系數矩陣a （ x ， u ）的特徵值實部大於零的區域）時散度型方程組（ 2 ）解的局部解存在性。在我們應用h . amann的局部解存在性理論時，我們發現h . amann的關于散度型方程組（ 2 ）局部解存在性理論的證明並不完整。
  11. Icso values of tps and egcg against d6 and wi - 38 are 71. 1 u g / ml, 1786. 7 u g / ml and 58. 6 u g / ml, 2177. 4 u g / ml respectively. lower concentrition of tps and egcg increased the number of wi - 38 and higher concentrition of tps and egcg also can inhibit the growth of wi - 38 cell and is concentration - dependent

    Egcg作用d6細胞后採用hoechst33258熒光染料染色並且在熒光顯微鏡下觀察，發現隨egcg作用濃度的增大，細胞出現染色體邊集、 dna斷裂、染色質環化等現象，而對照細胞的細胞核質呈現均一的顏色。
  12. Huwentoxin xi also have a strong biological activity with a ld5n = 256 u g / kg when injected into the fourth ventricle of the adult mouse brain

    Hwtx -對昆明種小白鼠第四腦室注射表現出較強的活性，其半致死量ld _ （ 50 ）為256ug kg 。
  13. Then the nucleuses were splitted by sds, dna was precipitated by iso - propanol or alcohol. the average dna yields were 527 u g / g with fresh base

    基因組dna平均得率為527 g g鮮重，經鑒定適合進行限制性酶切和rapd擴增。
  14. 5. da release from amy of female and ovx rats significantly increased in 5min after i. c. v injection of soy isoflavones at a dosage of 66. 7 u g / kg and declined to the control level within 20min

    7vn kn ）也在注射后smin內使雌鼠和ovx鼠的amyda釋放量明顯增加， 20min后恢復到對照組水平。
  15. The complex and the filter are dissolved in a small volume of dmso, and the absorbance of the resulting solution is measured by means of spectrophotometric method at 545nm wavelength against the reagent blank. the detection limits better than 1. 0 u g / l can be achieved

    50倍富集時，方法的檢出限為0 85pg l 。以上兩種方法應用於分析天然水以及礦泉水中的mo （ vi ）和的o ） ，回收率好，結果滿意。
  16. The optimum conditions of dot - elisa was determined : the optimal coating concentration was 8. 9 u g / ml, 1 : 400 was the best working concentration of hrp - laleled rabbit antichicken igg, the other steps and reagentes were also optimized

    抗原最適包被濃度為8 . 9 g / ml ，酶標抗體最適工作濃度為1 ： 400 ，確定了其他反應試劑和各步的最佳反應時間。
  17. 3 ) the donor of sd rat fibroblast cells, which had been treated with serum starvation for 3 - 5d, the 10 u g / ml of nocodazole and control, were used to recombine rat - mouse nuclear transfer embryos

    未經處理、血清饑餓3 - 5d 、 10 5 g mlnocodazole處理的大鼠成纖第四軍醫大學碩士學位論文雛細胞做供體構建重組胚胎，分別得到4 14 、 6 45 、 2
  18. At the same time, we get some new characterization of supersolvable and nilpotent groups by introduce the new concepts of u ( g ) and v ( g ). the following theorems are some of the main results in this thesis. 1

    特別地，引進群g的兩個特徵子群u （ g ）及v （ g ） ，用這兩個子群來刻劃有限群的結構，得到了有限群超可解，冪零的一些充分條件，減弱了某些已知定理的條件
  19. The ros level in cells treated with 80 u g / ml egcg increases 88. 9 % than that in control cells indicating that ros is connective with apoptosis in d6 cells

    通過檢測egcg處理d6細胞后ros的變化，發現80hg inlegcg誘導d6細胞凋亡時產生的ros是對照的188
  20. Typical apoptotic characteristics of d6 cells were determined by fluorescent microscopy and dna fragment electrophoresis after the cells were treated with egcg for 80 u g / ml for 48h

    以上結果表明， egcg在一定濃度和時間條件下，可以誘導d6細胞凋亡，並且以在濃度為80vg inl作用48h效果最好。
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