熒光染料 的英文怎麼說

中文拼音 [yíngguāngrǎnliào]
熒光染料 英文
flourescent 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...
  • 料 : 名詞1 （材料; 原料） material; stuff 2 （喂牲口用的穀物） feed; fodder 3 （料器） glassware 4 （...
  • 染料 : colourant; tincture; dyestuff; dye
  1. The progress of research on labeling of aberrant cell tissue by fluorescent probe or by connecting with biologically active carrier is reviewed

    簡述了熒光染料探針分子用於變異細胞組織的標記與識別的研究新進展。
  2. 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。
  3. The ultrafast dynamics of oxazine 750 dye has been studied in the typical alcoholic solvents by using the femtosecond time - resolved stimulated emission pumping fluorescence depletion ( fs tr sep pd ) technique

    摘要利用飛秒時間分辨熒光虧蝕光語技術，研究了惡嗪750激光染料分子在典型的醇類溶劑中超快動力學過程。
  4. Total cellular rna were extracted, 40 micrograms of the total rna were used in the reverse transcription reaction, using superscript ii reverse transcriptase, oligo ( dt ) i8 primers, and cy3 - dctp or cy5 - dctp for the experimental and control group respectively. the labeled cdnas were hybridized to microarrays at 42c for 12 h - 18 h

    提取as _ 2o _ 3作用k562細胞前後的總rna ，用superscript逆轉錄酶逆轉錄成cdna第一鏈，並在逆轉錄的過程中，用cy3 cy5熒光染料分別標記對照組處理組，與自製的k562細胞基因表達譜晶元雜交。
  5. 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。
  6. In comparison with common organic dyes, this class of fluorescent labels is 20 times as bright, 100 times as stable against photobleaching

    這種熒光標記物的發射光強是常用有機熒光染料的20倍，穩定性是其100倍。
  7. 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 。
  8. Standard practice for detection of mycoplasma contamination of cell cultures by use of the bisbenzamide dna - binding fluorochrome

    用二苯甲酰胺與dna結合熒光染料法檢測細胞培養中枝原體屬染菌的標準實施規程
  9. 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。
  10. 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。
  11. 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。
  12. The interaction of organogermanium with nucleotides is not soecific through the fluorometric test using different fluorometric stains, eb and dapi

    並且從不同熒光染料的熒光試驗得出二氯二乙基鍺與dna相互作用沒有堿基特異性。
  13. In chapter 3, a chemiluminescence biosensor on a chip coupled to microfluidic system is described in this paper. the chemiluminescence biosensor measured 25 + 45 + 5mm in dimension, was readily produced in analytical laboratory. glucose oxidase ( god ) was immobilized onto controlled - pore glass ( cpg ) via glutaraldehyde activation and packed into a reservior

    鐵氰化鉀熒光染料化學發光體系屬于首次報道，通過對該類體系的化學發光光譜的分析，發現該類體系的共同特點是，鐵氰化鉀氧化多酚類化合物，產生的能量轉移給熒光染料，然後產生強烈發光。
  14. And the mechanism of action of medicine to cell can be researched form biomedicine ; ( 3 ) the ca2 + concentration in b16 cell was measured with ratio fluorescence imagemaster. the preparation of cell and the carry method of fluorescence indicator were confirmed ; the acquisition of cell image and the ratio analysis method by software - imagemaster were established ; the acquisition of cell fluorescence image and the ratio analysis method by software - felix were established

    （ 3 ）通過用fura - 2 / am對b16細胞內ca ~ （ 2 + ）濃度的測量，確定了b16細胞的制備及熒光染料的載入方法；建立了用隨機軟體imagemaster獲取被測細胞的圖象及進行比率分析的方法，用隨機軟體felix獲取被測細胞的熒光圖譜及進行比率分析的方法。
  15. We also discover that luminous efficiency is increased markedly and two zones emission phenomenon appears if a fluorescent dye is added to the transitional layer between the etl and htl

    我們還發現，在互摻過渡層中再摻入熒光染料，能夠顯著提高器件的效率，並且觀察到了雙區域發射現象。
  16. The structure characteristics of aberrant cell, identification marking, fluorescence labeling technologies and methods of cell labeling by fluorescent probe are recommended

    介紹了變異細胞的結構特徵、細胞識別與熒光標記技術以及熒光染料探針分子標記細胞的方式。
  17. 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。
  18. 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。
  19. The third chapter : studying three mutually doped transitional layer structures " effects on the performance of oled. the three structures are the thin mutually doped transitional layer with concentration gradually changing structure, the thicker transitional layer with uniform concentration structure and the transitional layer doped with fluorescent dye structure

    第三章：研究了短距離內濃度漸變互摻、較長距離的均勻比例互摻以及通過摻雜熒光染料進行互摻的三種互摻過渡層結構對器件性能的影響。
  20. The development of new fluorescence dye and imaging technique have greatly promoted the research in the field of cellular calcium signal transduction path

    新的熒光染料的開發和成像技術的發展，極大的促進了對細胞內鈣信號傳導途徑的研究。
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