熒光顯象 的英文怎麼說
中文拼音 [yíngguāngxiǎnxiàng]
熒光顯象
英文
flucorescent imaging-
Tb substitution of pb induces lattice aberrance. this not only lowers the crystallization ability, butalowers the tetragonality of the powders as well
研究發現pt / tb體系中出現了顯著的tb離子特徵熒光和pb離子的熒光現象。High - powered technology of tricolor fluorescent powder and trioxide aluminum envelope mix powder make the products effective, durable, high luminosity, long life, unshadowed, no black head phenomena, good color rendering and less eyestrain
燈管採用高性能的三基色熒光粉及三氧化鋁包膜配粉技術，光效高，壽命長，無暗區，無黑頭現象，顯色性好，保護視力。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。Inhibition by zn2 + and mn2 + additive, and almost 100 % of t he activity was inhibited under their physiologically significant concentrations. these results suggest that the protease is possibly regulated by divalent cations in vivo
蛋白酶的活性受到某些二價金屬陽離于的抑制，比如zn訃、 mg卜、 hg熒光發射光譜結果顯示，在不同的抑制劑作用下，蛋白酶的高級構象可能發生了較大變化。Phosphors for color picture tubes use - phosphor y22 - b2
彩色顯象管用熒光粉y22 - b2熒光粉By compressing a monolayer film, the coexistence of liquid condensed ( lc ) and liquid expanded ( le ) phases can be reached. the transition from le to lc is usually regarded as a first - order one, so the theory of crystallization can be applied. in this article we review our recent studies on the growth of lc domains in the le - lc coexistence region driven by the illumination of a fluorescent microscope. the mechanism of this unusual 2d domain growth phenomenon is discussed. the formation of faceted, dendritic and fractal - like domains as well as the evolution and the transition of these patterns are investigated
當處于氣液界面的類脂類化合物的單分子膜被壓縮時，隨著分子間距的縮小，單分子膜將經歷一系列相變過程.通過熒光顯微術可以觀測到新相的成核和生長過程.由於單分子膜的二維特性，該系統中的實驗觀測對于檢驗和發展二維界面生長理論尤為重要.本文總結了近年來本課題組與相關單位合作，在單分子膜系統中發現的實驗現象以及對其生長機制的系列研究.內容包括對單分子膜系統中的成核、界面穩定性、枝晶生長、形態演變等的觀測和分析Abstract : by compressing a monolayer film, the coexistence of liquid condensed ( lc ) and liquid expanded ( le ) phases can be reached. the transition from le to lc is usually regarded as a first - order one, so the theory of crystallization can be applied. in this article we review our recent studies on the growth of lc domains in the le - lc coexistence region driven by the illumination of a fluorescent microscope. the mechanism of this unusual 2d domain growth phenomenon is discussed. the formation of faceted, dendritic and fractal - like domains as well as the evolution and the transition of these patterns are investigated
文摘:當處于氣液界面的類脂類化合物的單分子膜被壓縮時，隨著分子間距的縮小，單分子膜將經歷一系列相變過程.通過熒光顯微術可以觀測到新相的成核和生長過程.由於單分子膜的二維特性，該系統中的實驗觀測對于檢驗和發展二維界面生長理論尤為重要.本文總結了近年來本課題組與相關單位合作，在單分子膜系統中發現的實驗現象以及對其生長機制的系列研究.內容包括對單分子膜系統中的成核、界面穩定性、枝晶生長、形態演變等的觀測和分析The approaches used in the study included : observing the microstructure and ultrastructure of the cell line of colossoma brachypomum ( cbt ) and the cell line of carp ( cp ) stressed low temperatures under fluoroscopy and tem ; analysis of dna damage in the cultured cells under temperatures stress by dna gel electrophoresis
本研究採用的主要實驗方法：通過熒光顯微觀察、電鏡超微結構觀察確定cbt （淡水白鯧臀鰭細胞）和cp （草魚胚胎細胞）在低溫處理后的顯微與超微結構的變化。應用dna電泳分析細胞dna在低溫處理后的斷裂現象。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 。Phosphors for color picture tubes use - phosphor y22 - g3
彩色顯象管用熒光粉y22 - g3熒光粉Fluorescence power transfer function, three - dimensional point spread function ( 3d - psf ) and three - dimensional optical transfer function ( sd - otf ) for the various fluorescent wavelength of the two kinds of fluorescence confocal scanning microscopy are calculated in this paper by using fourier imaging theory. the results show that the fluorescent wavelength has influence on imaging property of confocal microscopy such as spatial cut - off frequency, resolution and 3d - otf. there is a different missing - cone in the 3 - d space of otf when the ratio of excitation wavelength to fluorescent wavelength decreases
本文在sheppard和gumin等人的理論基礎上，利用fourier光學成像理論，討論了不同熒光波長對單光子和雙光子共焦顯微鏡成像特性的影響，導出了單光子和雙光子共焦顯微鏡的熒光功率傳輸函數、三維脈沖響應函數和三維光學傳遞函數，得到了它們在不同激發波長與熒光波長比值時具體的表達式，並且通過數值計算，得到了它們的曲線圖，結果表明：隨著激發波長與熒光波長比值的增加，焦斑的橫向分佈和縱向分佈變窄，橫向解析度和縱向解析度提高，系統的成像效果變好，當激發波長與熒光波長的比值下降到一定程度時，可以看到不同程度的失錐現象。Using the methods of fluoro - gold ( fg ) retrograde tracing combined with immuno - fluorescence histochemistry, cb - immunoreactive neurons expressed immunoreactivity for fos protein in nts which send their axons to bst were investigated. after injecting fg into bst mainly in lateral part, the fg retrogradely labeled neurons were found in the mid - caudal part of nts bilaterally with ipsilateral side predominance. cb - and fos - immunoreactive neurons were distributed equally in both sides of nts
結果顯示：將熒光金（ fg ）注入一側終紋床核外側部（ bstl ）后，中尾段nts內雙側出現fg逆行標記神經元，注射區同側占優勢； nts的相同平面可觀察到雙側等量分佈的兔疫反應陽性的cb和fos神經元：三種神經元的分佈有明顯的重疊現象。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。In our research, marked autologous fluorescent blood red cell is immitted into sd - rat body and the whole process is shown and recorded by microscope image system. after these processes, we can replay the recorded tape and sample images with video image card. then, we use sequence image processing to analysis the image of dark ground microscope
利用做過熒光標記的自身紅細胞注入sd大鼠體內，通過顯微圖象系統將整個過程以視頻信號的形式存貯，然後利用基於視頻圖象的採集卡，將流速變化過程回放采樣，得到暗視場下的熒光圖象，利用圖象分析和處理的方法，測定血流速度。The algorithm of sequencable mark and description of the object for crack automatic identification is presented by means of pre - image process. on basis of visual c + + 6. 0 developing environment, the software function of controlling of magnetic partical testing engine and the stepping - motor is realized in c + + and mfc with objected programming method. the automatic system of the camshaft of small diesel engines automatic magnetic partical testing is realized, which is the predicted goal that we would achieve
用計算機控制磁粉探傷機和步進電機的工作；解決了jpeg圖象格式在windows系統中visualc + +編程環境下的壓縮轉換、顯示和處理的問題；結合數字圖象的預處理，提出了通過圖象分析自動識別裂紋的順序目標標記與描述演算法；基於visualc + + 6 . 0開發環境，用c + +語言和mfc類庫，採用面向對象的程序設計方法，用軟體實現了對磁粉探傷機和步進電機等硬體系統的自動控制功能；實現了柴油機凸輪軸熒光磁粉探傷系統的自動化，達到了預期的目標。Luminance : project light upon in the ultraviolet ray wave under have thin huang green arrive blue fluorescence, short - wave fluorescence not obvious, the x shoots line irradiation to descend also have no give out light phenomenon obviously
發光性：在紫外線波照射下有淡黃綠到藍色的熒光，短波熒光不明顯， x射線照射下也無明顯的發光現象。During the research, we used the diffraction of x - ray. sem ( scanning electron microscope ), electron micro - probe, petrographic analysis, cements physical performance test, adiabatic test, concrete test and so on, also, we gave explanations to all kinds of expansion phenomenon
本課題在研究過程中採用了x ?射線衍射掃描電子顯微鏡、電子探針、 x ?熒光分析、巖相分析、水泥物理性能試驗、絕熱試驗、混凝土試驗等手段，對各種膨脹現象作出了解釋。The sem and the pl observation showed that the surface of porous silicon prepared by pulsed etching was more uniform and the si particles were smaller. the intensity of pl formed by pulsed etching method was enhanced and the peak had blue shift comparing that formed by dc electrochemical etching method. at the same time, it was observed that the smaller the dimension of the porous silicon, the broader energy gap of the porous silicon
採用脈沖和直流電化學腐蝕兩種方法制備多孔硅，對這兩種方法制備的多孔硅樣品進行掃描電鏡和熒光光譜的測量，發現脈沖腐蝕制備的多孔硅樣品比直流腐蝕制備的多孔硅樣品表面均勻、顆粒尺寸小、發光強度大，而且發光峰位有明顯的藍移現象。3, by immunofluoresent microscopy, we also found that brg1 did not clearly co - localize with rna polymerase ii small subunit b6, but partially co - localized with rna polymerase ii small subunit b8 ; nf1 / ctf clearly co - localized with rna polymerase ii small subunit b6 and partially with b8. these data implies that brg1 may be partially associated to b8 and nf1 / ctf may be involved in the formation of transcription initiation complex through associating to brg1 and b6
3 、通過兔疫熒光實驗我們還發現， brg和rna聚合酶d亞基b6之間沒有明顯共定位現象，與rna聚合酶11小亞基bs有部分的共定位現象：呷1兒仆與刪a聚合酶小亞基孤有比較明顯的共定位，與rna聚合酶11小亞基bs有部分的共定位。In order to investigate the effects of ph, temperature, naf and bivalent cations on the conformation of the phosphatase in solution, we monitored the difference of intrinsic fluorescence of the phosphatase and compared changes of the enzyme activity under those conditions. the tertiary structure loosed and the intensity of fluorescence decreased below ph 6. 0. the intensity of fluorescence was lowest at ph 5. 0 and the tertiary structure was reconstructed as the solution ph was increased
其中在ph5 . 0及以下時，蛋白質的三級結構變得鬆散，熒光強度下降， ph5 . 0時尤為顯著，而當溶液ph高於5 . 0時（酶的最適ph ） ，樣品的熒光發射強度明顯增加，表明酶蛋白受溶液酸堿度的影響，構象發生部分變化，部分trp殘基向疏水環境移動，其三級結構得到恢復。分享友人