blue fluorescence 中文意思是什麼

blue fluorescence 解釋
藍色熒光
  • blue : adj 1 青，藍，藍色的，天藍色的；（臉色）發灰[青]的，（皮毛等）青灰色的。2 陰郁的，憂郁的，沮喪的...
  • fluorescence : n. 熒光（性）。
  1. 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。
  2. Based on the analysis and summary of related literature, three organic and polymer electroluminescence ( el ) materials have been synthesized. one copolymer consists of polyvinylcarbazole moiety, which can form high quality thin films with excellent hole - transporting function and binaphthyl moiety, which emits blue fluorescence

    其中，一個共聚高分子為分子中含有典型的空穴傳輸功能的乙烯基咔唑基團和有較好發光效率並能發藍光的聯萘基的非共軛聚合物（ dmbn - vcz ） 。
  3. Fluorescence tone : slight greenish blue

    熒光色調：微青色調。
  4. In this thesis the in situ brilliant cresyl blue ( bcb ) dimer with weak fluorescence in the solution of anionic surfactant ( as ) sodium lauryl sulfonate ( sls ) was used as fluorescence probe. at the same time, the new method for the determination of bovine serum albumin ( bsa ) was built. the linear range was 0 - 7mg / l and the detection limit ( 3 o / k ) was 3. 66 10 - 3 mg / l, the r. s. d for the determination of 2. 00mg / l bsa was 2. 77 %

    本論文以陽離子染料燦爛甲酚藍在陰離子表面活性劑十二烷基磺酸鈉存在下形成的現場弱熒光二聚體為熒光探針，建立了測定牛血清白蛋白的新方法，該法線性范圍為0 7mg / l ，檢測限為3 . 66 10 ~ （ - 3 ） mg / l ，對2 . 00mg / l幾的牛血清白蛋白平行測定8次，相對標準偏差為2 . 77 ，說明本法準確可靠。
  5. Under that condition the strain can produce the most concentration of the bioactive compounds. the physical and chemical properties of the actibacterial compounds have been studied, the results showed the bioactive substance has heat stable, acidity and weakly alkali stable. it can be dissolved in acid water, chloroform solvent, can not be dissolved in ethyl acetate, petroleum ether, alkali water. the result of thinlayer chromatography showed the bioactive compounds can give off blue and green fluorescence in the uv light. the paper chromatography demonstrate the bioactive substance may be a new construct compounds

    研究表明，該活性物質具有較強的熱穩定性， ph 9的條件下能穩定存在，但ph 12的強堿性條件下活性物質的抗菌活性幾近喪失；活性物質易溶於氯仿、酸性水、不溶於乙酸乙酯、石油醚、堿性水；薄層層析顯示活性物質在紫外光下能發藍綠色熒光等特點；由捷克八溶劑系統紙層析鑒定該抗菌活性物質不屬於四大類抗生素，可能為一新的抗菌活性物質。
  6. Green fluorescent protein has several good characters. under excitation of long uv light or blue light, it emits green fluorescence without requiring any exogenous substrates and cofactors. gfp gene expression can be used to monitor gene expression and protein localization in living cells and organisms. this is a development of revolutionary significance. the dna sequence of this gene can be re - engineered by mutagenesis and the gfp will get improved fluorescent properties. the applications of gfp will be wider and wider

    綠色熒光蛋白具有優良的特性，在藍光或長紫外光的激發下，不需要任何外源底物或內源輔助因子的參入就能發出綠色熒光.綠色熒光蛋白基因的表達可用來監控活細胞或生物體中基因表達和蛋白質的定位.這是一個革命性的進展.而且，對基因dna序列的改造有可能使綠色熒光蛋白的發光特性更加優良，從而其應用范圍會更加廣泛
  7. With strong fluorescence lppp showed a broad pl and el emission with a maximum at 560nm and was regarded as a white light emitter with a strong blue component, thus allowing tunability over the full visible region. the enhanced light - emitting devices were fabricated. microcavity effects were observed both in el and pl

    熒光效率高，並具有從紫外到近紅外十分寬闊的光致和電致發光光譜，最大峰值在560nm左右，是一種具有較強藍光成分的白光發光材料，允許在整個可見光范圍內進行調諧發光，可作為高穩定的發光材料。
  8. Paper and board tests. assessment of the contribution of fluorescence in the measurement of the diffuse blue reflectance factor

    紙張和紙板試驗.評估螢光在測量藍色漫反射系數時的作用
  9. So the method was accurate and reliable. the in situ nile blue ( nb ) dimer with weak fluorescence in the solution of anionic surfactant sodium dodecylbenzene sulfonate - 6 ( dbss ) was also used as the fluorescence probe for the determination of total proteins in human serum

    以陽離子染料耐爾藍在陰離子表面活性劑十二烷基苯磺酸鈉存在下形成的現場弱熒光二聚體作為測定人血清總蛋白的熒光探針。該法用於實際樣品的測定，與臨床方法測定的結果相吻合。
  10. By the former experiment, we know that the fiber optic gas sensor with the pulse light of the blue light led can emit the steady fluorescence. so we can detect the density of oxygen through

    技術方案上採用數字脈沖激勵led藍紫光源照射敏感元件獲得穩定的熒光信號，再通過測量熒光壽命檢測氧氣濃度。
  11. The fluorescence spectrum ( fls ) of lra excited at 280nm and 295nm showed a maximum peak at 338nm. the characteristic peak of tyr did not exist, and it showed that the fluorescence energy of tyr was transformed to trp and strength the fluorescence of trp. when lra was excited at 295nm, the fls showed a maximum peak at 338nm, the max of fluorescence emission spectrum blue - shifted more than 10nm compared with the max of free tyr ( 348nm )

    Lra的熒光光譜研究表明在激發光波長為280nm時，其最大熒光發射峰在338nm處，熒光光譜未見有酪氨酸（ tyr ）殘基的發射峰，表明tyr殘基的熒光基本上通過能量轉移到trp上，使熒光強度增強，在激發光譜為295nm時，其最大熒光發射峰338nm ，比游離trp的最大熒光發射峰（ 348lun ）藍移了近10nln ，說明trp周圍的極性較弱，處于疏水的微環境。
  12. 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。
  13. At first, we investigated the photoluminescence characterization of theion - implanted samples by spectroanalysis, found that the ion implantation would damage the crystal lattice structure and affect the optical radiation of characteristic. moreover, the crystal lattice structure will be restored after annealing, which can be determined by the change of fluorescence peak intensity and blue migration of wavelength

    發現mn ~ +離子、 c離子的注入都會損傷樣品的晶格結構，從而影響樣品的發光特性，而退火處理對這些損傷有一定的修復作用，這可以從發光峰強度的變化及波長的藍移來判定。
  14. It is interesting to find that the green - emission band in solvent solution has been quenched, meanwhile, the blue - emission band appeared at the present of b - cd, suggesting that molecular materials have sensitive to the micro - circumstance and have potential application for fluorescence probe

    這種由極性環境到非極性環境引起的發射光峰位明顯變化特性，即對微環境的敏感性，具有作為熒光探針的潛在性能。
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