fluorescence intensity 中文意思是什麼
fluorescence intensity
解釋
熒光強度- fluorescence : n. 熒光（性）。
- intensity : n. 1. （思想、感情的）強烈，激烈。2. 強度。3. 【攝影】（底片的）明暗度。
-
[ result and discussion ] 1. combination between 2 - amac labeled oligochitosan and macrophage : 2 - amac - oligochitosan first bound the cytomembrane of macrophage, and then diffused in the whole cytoplasm, at last entered the nucleolus and diffused in the whole cell. fluorescence intensity increased with time
2 -氨基吖啶酮標記的殼寡糖與巨噬細胞的結合情況： 2 -氨基吖啶浙江大學碩士學位論文酮標記的殼寡糖先與巨噬細胞膜有結合，然後分佈於整個細胞質，最後進入細胞核，隨時間的進展而呈現了一個內在化過程。 -
Though zn 2 + and co 2 + are divalent ions, they probably can not substitute ca2 + from the active center of tcs, or can substitute ca2 + but does not change the structure of tcs. there is no significant change observed for the fluorescence intensity of tcs
『 「是二價金屬離子，但這兩種離子與天花粉蛋白作用時可能並沒有取代天花粉蛋白活性部位的ca 『 」 ，或部分取代但並沒有改變天花粉蛋白分子的空間結構，以致天花粉蛋白的熒光強度無明顯變化。 -
Meanwhile, after aba induced the h2o2 accumulation in guard cells, the exogenous or intracellular pd98059 could reduce the dcf fluorescence intensity
與aba一樣sa誘導了保衛細胞中dcf熒光強度迅速升高。 -
In order to study the mechanism of the effect of low concentration tfp on the proliferation of s. pombe, we watch yeast cells loaded with fluo - 3 under laser scanning confocal microscope ( lscm ). the fluorescence intensity reflected the cytosolic free calcium concentration. the result showed that, the cytosolic free ca2 + concentration in s. pombe cultured in ca2 + - free medium was 2 ~ 3 times lower than that in s. pombe cultured in medium containing 10umol / l ca24, while ca2 + concentration in s. pombe treated with 50umol / l tfp was 4 - 5 times higher
本文發現增加胞外鈣濃度以及低濃度（ 20 100 mol l ）三氟拉嗪（ tfp ）不但能促進野生型s . pombe細胞的增殖，而且對mfp7菌株也有同樣的效應，這說明胞外ca ~ （ 2 + ）和低濃度tfp對不同遺傳型裂殖酵母細胞的增殖均有促進作用。 -
We used fission yeast schizosaccharomyces pombe ( s. pombe ), an unicellular eukaryotic organism, as research material. electroporation was adopted to load ca2 + fluorescent indicator into yeast cell and under the laser scanning confocal microscopy ( lscm ), we observed cytosolic ca2 + distribution and relative content as well as fluorescence intensity of gfp - cam in different phases of cell cycle of yeast cell. flow cytometry provided a way of determining the relative dna content of populations of fission yeast
本文以單細胞的真核模式生物裂殖酵母（ schizosaccharomycespombe ）為研究材料，通過激光掃描共聚焦顯微鏡觀察酵母細胞胞質內游離ca ~ （ 2 + ）的分佈及相對濃度，以及不同周期時相細胞中gfp - cam的熒光強度變化，並採用細胞流式法對酵母細胞的相對dna含量進行測定以確定細胞所處周期時相。 -
3. observe the binding of oligochitosan labeled with 2 - amac with macrophages under confocal laser microscope and analysis the fluorescence intensity by flow cytometer using the cell quest software
在激光掃描共聚焦顯微鏡下觀察2 -氨基吖啶酮標記殼寡糖與巨噬細胞的結合，用流式細胞儀分析熒光強度。 -
Stable fluorescent labels bhhct - eu3 +, bpta - tb3 ", and europium nanoparticle were used to develop sandwich - type time - resolved fluoroimmunoassays for hbsag. fluorescence intensity was directly detected on the surface of the solid phase
利用穩定的稀土標記物bhhct - eu3 + 、 bpta - tb3 +和銪納米顆粒建立夾心型固相時間分辨熒光免疫分析（ trfia ）直接定量測定乙肝表面抗原（ hbsag ）的新方法。 -
In the theoretical description of grazing emission fluorescence, the mode of fluorescence intensity emitted from layered materials dependence of grazing angle is established by applying asymptotic approximations to double fourier integrals, and the theoretic calculation formula of fluorescence intensity from a thin layer is derived. by the derived expressions, the theoretic simulation curves of several thin layers on si substrate are calculated. in the experimental setup, the requirement of construction of the setup and some important parameters are brought forward
最後，利用平穩位相方法建立了掠出射情況下薄層樣品產生的熒光強度和掠出射角的對應關系數學模型，推導了薄層樣品熒光強度理論計算公式，並以此為依據模擬計算得出了cr 、 fe 、 ti和ni等幾種以si作基底的單層薄膜樣品的熒光強度隨掠出射角變化的理論曲線。 -
When the probe was exposed to dissolved ammonia, ammonia would enter into the probe through the pore and react with the indictor, and then the fluorescence intensity of the indictor would increase
氨通過孔洞進入探頭內部與指示劑作用，引起指示劑熒光強度的變化，從而達到對氨測量的目的。 -
The results indicated that the content of cytosolic cam in cells treated with exogenous ca2 + has increased indistinctively, while fluorescence intensity in cells treated with tfp decreased. so we believed that exogenous ca2 + has little effect on the expression of cam
結果發現，經過外鈣處理的酵母細胞胞內cam的表達量有所增加，但並不明顯，因此認為增加外鈣濃度對胞內cam的表達影響不大，但使處于活化態的cam相應增加。 -
The fluorescence intensity of pb became weak when the crystal phase began to form in tha the lattice vibration absorbed the energy induced by the fluorescent transition
隨著體系中晶態的生成， pb離子進入晶格中，由於晶格振動所產生的聲子吸收了躍遷回落產生的發光能量， pb離子的熒光強度明顯下降。 -
This demonstrates the feasibility of using grazing emission x - ray fluorescence spectroscopy as a method of studying the thin layer ' s characteristics, such as composition and thickiness etc. with the intimately combining of theoretical, set - up and experimental research, the study on the analysis techniques of grazing emission x - ray fluorescence is developed, and the first set of grazing emission x - ray fluorescence setup is established. at the same time, the angular dependence of the fluorescence intensity with different thickness layer is measured. all the work in this thesis provides the basis for the further researches
本論文採用理論、裝置和實驗研究密切結合的方式，開展了掠射x射線熒光分析技術研究工作，在國內建立了首臺掠出射x射線熒光光譜分析裝置，並對不同厚度單層和雙層薄膜樣品在掠出射條件下產生的熒光光強與掠射角的對應博士學位論文:掠射x射線熒光分析技術研究關系進行了實驗測定。 -
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 。 -
At that time, cytosolic fluorescence intensity decreased to normal level, which shows that most of cells get through the gl / s point and enter the log phase. when cultured in medium that neucl was omitted, most of the cells were synchronized at gl stage of cell cycle. with flow cytometry, we found that cytosolic cam content of gl cells was higher than that of normal cells at log stage
在激光掃描共聚焦顯微鏡下觀察不同周期時相裂殖酵母細胞中cam的濃度及分佈變化，結果表明，分裂期細胞總體熒光強度強于間期細胞；而對同一細胞內熒光強度的分析說明，間期細胞的熒光主要分佈於胞質中，細胞核內則分佈較少；而正在進行有絲分裂的細胞內熒光主要集中於赤道板處；剛完成有絲分裂的細胞內熒光則相對集中於兩端或其中的一端。 -
The obtained recombinant - 5 - htr plasmid was tranfected into human liver cancer smmc - 7721 cells. all data suggested the expression of plncx - atr could condense cell nucleus and increase nuclear fluorescence intensity, effectively repress the telomerase activity, cell growth and cell proliferation, and induce cell apoptosis
反義重組質粒plncx - atr轉染人肝癌smmc - 7721細胞，結果發現plncx - atr的表達有效地封閉或抑制肝癌細胞的端粒酶活性，使細胞的生長和增殖受到抑制，細胞體積變小、核緻密、核熒光強度增強，且促進其凋亡。 -
Experimental result indicated that this compound has a strong chelating ability to ca2 +, and the fluorescence intensity of this compound was increased with the increase of ca2 + concentration under suitable conditions
結果表明， 4 - bapta對ca ~ 2 +具有很強的絡合能力，而且在一定條件下它的熒光強度隨鈣離子濃度增加而增強。 -
The fluorescence intensity of tb observed in pt / tb sol was stronger than that in powders. the network made of o, ti, such as sol and noncrystalline powders, determined the fluorescence intensity of pb
Pb離子的熒光與pb所處環境相關，既可出現在液相體系，又可出現在固相粉末體系中，也即處于o ， ti等離子構成的無規則網路結構狀態下的溶膠、凝膠或非晶固態時。 -
The result of fluorescence show that the fluorescence intensity of the surface of the treated glass slide connect with the probe immobile ratio of oligonucleotide. the more oligonucleotide probes have been linked with active group, the stronger fluorescence intensity is. for the strongest fluorescence, the technical conditions is : treatment of 2 % aminosilane of 20 minutes, treatment of 5 % aldehyde of 24 minutes, uv crosslinking of 150mj and washing of 5 minutes at 20
兩種檢測方法表明，當活性基團呈柱狀、分佈均勻且尺寸比較大（ 200nm ）時，有利於寡核苷酸探針的連接，且連接探針數量多，玻片表面熒光強度強，固定率高；當活性基團呈錐狀、分佈及尺寸不均勻（ 150nm （ 300nm ）時，連接的寡核苷酸探針數量少，玻片表面熒光強度弱，固定率低。 -
P - n, n - dimethlaminobenzates ( ( ch3 ) 2nc6h4coor ) have typical ict characteristics. the ct emission and the fluorescence intensity ratio of ct band to normal band ( ict / ile ) were different in organic solvent and in the aqueous solvent with ctab micelle when the length of r group was increasing
N ， n -二氨基苯甲酸酯系列具有典型的雙熒光，從甲酯到辛酯隨著酯烷基鏈的增長，它們在有機溶劑和膠束水溶液中的熒光峰位置以及雙重熒光強度之間的比值不同。 -
As heavy oil has fairly high aromatic hydrocarbon compound characterized by a wide range of components, the application of three - dimensional fluorescence pattern composed of excitation wavelength, emission wavelength and fluorescence intensity can detect the composition, intensity and characteristics of aromatic hydrocarbon compound
摘要根據重質油含有芳香烴化合物的組成范圍很寬、含量較高的特點，應用由激發波長、發射波長和熒光強度組成的三維熒光圖譜，可以檢測芳烴化合物組成、強度及其特徵。
分享友人