熒光染色 的英文怎麼說

中文拼音 [yíngguāngrǎnshǎi]
熒光染色 英文
fluorescent dye
  • 熒 : 形容詞[書面語]1. （光亮微弱的樣子） glimmering 2. （眼光迷亂; 疑惑） dazzled; perplexed
  • 光 : Ⅰ名詞1 （照耀在物體上、使人能看見物體的一種物質） light; ray 2 （景物） scenery 3 （光彩; 榮譽） ...
  • 染 : Ⅰ動詞1 （用染料著色）dye 2 （感染） catch [contract] （a disease） 3 （沾染） acquire （a bad hab...
  • 色 : 色名詞[口語] （顏色） colour
  • 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
  1. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的：構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體外轉染膀胱癌biu - 87細胞后，利用赤潮毒素作用后細胞表達綠色熒光蛋白的變化來檢測赤潮毒素，初步建立一種以細胞為基礎受體水平的赤潮毒素檢測方法。
  2. 6. oocytes were fixed for immunofluorescence. examination of cgs and microtubules were performed by fitc labeled lens culinaris agglutinin ( lca ) and and - fi - tubulin under confocal scanning laser microscopy ( cslm ) respectively

    利用直接免疫熒光染色和共聚焦顯微鏡（ confocalscan muglasermicroscopy ， cslm ） ，研究各組體夕成熟卵的皮質顆粒和微管
  3. Observations with fluorescent staining of amitosis in nitellopsis obtuse

    熒光染色觀察鈍節擬麗藻中無絲分裂的研究
  4. Mycobacteria can also be stained with auramine and viewed with fluorescence microscopy, in which acid fast bacilli now appear as glowing yellow rods

    分枝桿菌也能被金胺染色，熒光顯微鏡下抗酸桿菌為發黃*色熒光的桿菌。
  5. Materials and methods the mouse, golden hamster and human sperm were incubated with endotoxin in different concentration for different time to get capacitation, respectively, and ar was induced by progesterone after capacitation, then the rates of capacitation and ar were detected by chlortetracycline ( ctc ) and hoechst 33258 fluorescent staining method. the medium was with endotoxin in different concentration in sperm - oocyte fusion step during ivf, then the fertilization rate was observed. the 1 - cell, 2 - cell and zona - free 2 - cell mouse embryos were incubated in the medium with endotoxin, then the rate of blastocysts was recorded

    方法取小鼠精子10份、金黃地鼠精子6份、人新鮮精液標本10份及人冷凍精液標本9份，分別與不同濃度內毒素共孵育進行體外獲能和孕酮誘導的頂體反應，應用金黴素和dna結合的熒光染料hoechest33258雙重熒光染色法檢測精子的獲能率和頂體反應率；小鼠體外受精實驗的精卵結合環節培養液中加入不同濃度的內毒素，觀察受精情況並記錄受精率；取小鼠1 -細胞胚胎、 2 -細胞胚胎和去卵透明帶2 -細胞胚胎，與不同濃度內毒素共孵育進行體外培養，觀察體外發育情況並記錄囊胚率。
  6. To investigate the consequence of this interaction, aes - rfp fusion protein expression vector was constructed and co - transfected into nih 3t3 cells with tle1 - gfp fusion protein expression vector. confocal microscopy observation showed that aes could interact with tle1 at the cytomembrane region. moreover, this interaction inhibited the concentration of tle1 into nucleus

    在構建了紅色熒光蛋白aes表達載體后，將其與tle綠色熒尤蛋白載體共轉染細胞，共聚焦顯微鏡觀察發現這兩種分子在胞漿中有共存現象，而且aes的表達可抑制tlei向胞核內的聚積。
  7. The cell microarrys were dyed with trypan blue, wrights, three colors fluorescence and papanicolaou strained. results leukocyte samples from 20 all patients showed predictably and distinctly different dot patterns from samples from 20 normal subjects

    將雜交后的細胞晶元進行胎盤蘭染色、瑞氏染色、 cd3 cys cd4 fitc cds rpe三色熒光染色、巴氏染色等並觀察結果。
  8. If an immunofluorescence stain with antibody to complement or immunoglobulin is performed, then one can see the brightly fluorescing band along the dermal epidermal junction that indicates immune complex deposits are present

    如果針對補體的抗體或免疫球蛋白進行免疫熒光染色，我們就能在表皮與真皮的交界處看到一條明亮熒光帶，表明有免疫復合物的存在
  9. Those of micro - ball with different fluorescent dye can be used in biochemical analyses and biology molecules will react on the micro - ball

    利用帶有兩種熒光染色劑的微球進行生物分析，生化反應將在懸浮於液體中的球基上進行。
  10. In our report, we selected trehalose to substitute sucrose in the cryoprotectant. the process of vitrification is under the same preferable condition. the survival - rate of the recovered cells was tested by fda - pi and cd34 + cell - count

    凍融后的細胞以fda - pi雙熒光染色、流式細胞儀cd34 +計數等檢測手段，與同樣條件的60蔗糖保護劑處理的細胞相比較。
  11. The survival - rate of the recovered cells was tested by mtt and fda - pi. therefore, we got the preferable condition of vitrification, i. e., the concentration of cryoprotectant is 60 % and the time of disposal is 15min. under this condition, the value of fda / pi is 46. 43

    凍融后的細胞經過mtt檢測和fda - pi雙熒光染色法檢測，獲得預處理過渡的優化條件，即60濃度的保護劑，預處理15分鐘，此時的fda pi值為46 . 43 。
  12. Throughout the culture period, most cells within the colonies continued to be alkaline phosphata se positive and specific stage embryonic antigen ( ssea - 1 ) positive which has been used routinely to characterize embryonic stem and pgcs cells

    經過4 7天培養， pgcs形成典型的鳥巢狀集落。集落在傳代過程中保持堿性磷酸酶活性，胚胎階段性特異抗原1 （ ssea - 1 ）免疫熒光染色顯示陽性。
  13. We studied development mechanism by the distribution of microfilaments and actin mrna in cotton callus, healtny plants and abnormal plantlets. fitc - phalloidin as fluorescence probe was used to investigate the meristem of the cotton root, abnormal plantlets and callus that was unable to germinate into healthy plants

    本研究選取正常棉花的根，已經培養了長時間不能分化出正常植株的棉花愈傷組織和棉花畸形苗為材料，採用石蠟切片，通過fitc -鬼筆環肽對材料微絲熒光染色，結合熒光顯微鏡觀察。
  14. A mixture of three amino acids ( arg, gly, glu ) labeled with fluorescein isothiocyanate ( fitc ) was separated in pdms microfluidic chip, the separation voltage is 200v / cm, the separation time is less than 120 seconds ; according to ccd fluorescence images, two distinct physical processes - stacking and destacking during sample injection were studied qualitatively ; rhodamine b, a kind of temperature - dependent fluorescence dye, was used as probe to develop a temperature - fluorescence intensity equation, then temperature - color map in microchannels was constructed, and temperature trait in microchannels on the pdms microfluidic chip was analysed. according to the results, we conclude that the electric field applied to the pdms microfluidic chip should not exceed 400v / cm

    利用pdms微流控晶元對fitc標記的精氨酸、甘氨酸、谷氨酸混合物進行了電泳分離，分離電壓為200v cm ，分離時間不到120秒；通過拍到的熒光顯微圖像對電泳注樣過程中復雜的樣品分子積聚與解聚現象作定性的分析；以熒光染料rhodamineb為溫度熒光探針，建立了pdms微流控晶元上的溫度-熒光強度的關系公式，並利用matlab圖像處理工具箱構建出微流體溝道內的溫度色圖，對pdms微流控晶元的微流道溫度特性進行了分析，根據實驗結果，我們認為對于pdms微流控晶元來說，在進行需要外加電場作用的試驗時，外加電場不應超過400v cm 。
  15. First we employed c. w. m2r, a fluorescent fabric brightener, to investigate changes of wall of female germ unit before and after fertilization

    通過熒光染色技術，我們首先觀察了自然受精過程中胚囊內雌性生殖單位細胞壁的變化。
  16. Sections were stained by he and were observed under light microscope. ( 4 ) observation on cell - matrix complex with confocal microscope. cell - matrix complex was stained by fluorochrome cfda - am ( loug / ml, looul ) after 7 days incubation, the sample was scanned by confocal microscope to observe cell - growth in the matrix

    細胞一多孔膜復合物的激光共聚焦顯微鏡觀察：取培養7天的細胞一多孔膜復合物，以10ug inl的熒光染料cfad am100ul染色，檄光共聚焦顯微鏡檢測激光激發的綠色熒光，掃描成像觀察活細胞生長倩況。
  17. 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。
  18. In recent years many organic dyes such as fluorescence dyes, laser dyes, nonlinear optical dyes and phototropic dyes were inducted into the inorganic matrix or ormosils

    各種熒光染料、激光染料、 nlo染料及光致變色染料等相繼被引入到無機基質或有機改性硅酸鹽中。
  19. We use a specific no probe diaminofluorescein diacetate ( daf - 2da ) to visualize the changes of no content with different treatments and its localization. the no burst in arabidopsis was induced by vd - toxin, sa and h2o2. no accumulated in the guard cells and the epidermal cells of the lower epidermal layer of arabidopsis

    用no特異熒光染料daf - 2da染色得知，毒素、 sa 、 h _ 2o _ 2單獨及組合處理擬南芥下表皮條均能誘導no的積累， no主要積累于在保衛細胞腹壁上，在保衛細胞的胞質和表皮細胞的胞壁及胞質中也有no的積累。
  20. One kind of micro - ball ( diameter of 5. 6 m ) is dyed using red fluorescent dye, the other is dyed using green fluorescent dye

    用紅光熒光染料對直徑約5 . 6 m聚丙烯酰胺球基進行染色，用綠光熒光染料對另一種球基進行染色。
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