熒光強度 的英文怎麼說

中文拼音 [yíngguāngqiáng]
熒光強度 英文
fi
  • : 形容詞[書面語]1. (光亮微弱的樣子) glimmering 2. (眼光迷亂; 疑惑) dazzled; perplexed
  • : 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) ...
  • : 強形容詞(強硬不屈;固執) stubborn; unyielding
  • : 度動詞[書面語] (推測; 估計) surmise; estimate
  1. 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。
  2. The results showed that the fluorescent intensity of dph decreased and the fluorescent intensity of mc540 increased under sound stimulation, which indicated that the vesicles got looser, the charge density of membrane surface and the plasmalemma hydrophobicity decreased but the membrane fluidity increased

    結果表明,聲波刺激使標記質膜的dph偏振值降低、 mc540熒光強度增加。表明一定和頻率的聲波刺激使質膜變的疏鬆,膜表面電荷密降低,疏水性降低,流動性增加。
  3. Flow cytometry measurements were done to detect the changing of fluorescent signal of the reporter strain and give expression situation to ybt indirectly. 7 eaggec hpi - positive strains revealed an enhanced fluorescence signal but 1 eaggec hpi - negative did not so

    3n ) ,將待測eaggec菌株的培養上清加入該報告菌株培養物中,用流式細胞術facs方法檢測報告菌株熒光強度的變化情況,間接反映ybt的表達與否。
  4. 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。
  5. 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,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。
  6. The purposes of the present study were to investigate ( 1 ) the hemodynamic effects of agmatine in anaesthetized dahl salt - sensitive ( ds ) hypertensive and dahl salt - resistant ( dr ) rats ; ( 2 ) the effect of agmatine on vascular tension in the isolated aortic artery of rats and the underlying receptor mechanism ; ( 3 ) the effects of local injection of agmatine on femoral, renal, and mesenteric vascular beds by constant flow perfusion method ; ( 4 ) the effect of agmatine on l - type calcium current ( / ca - t ) in rat ventricular myocytes with whole - cell configuration of the patch - clamp technique ; ( 5 ) the effects of agmatine on free intracellular calcium concentration ( ca2 + d of isolated rat ventricular myocytes

    ( 3 )採用後肢、腎臟和腸系膜動脈在體恆流灌注法,觀察向灌流環路中直接注射胍丁胺的血管效應。 ( 4 )應用全細胞膜片箝技術,觀察胍丁胺對大鼠心室肌細胞l -型鈣通道電流( i _ ( ca - l ) )的影響。 ( 5 )用fluo3 - am負載分離的大鼠心室肌細胞后,由激共聚焦法測定單個心室肌細胞[ ca ~ ( 2 + ) ] _ i的熒光強度,觀察胍丁胺對分離大鼠心室肌細胞內游離鈣濃( [ ca ~ ( 2 + ) ] _ i )的影響。
  7. We have prepared a series of neodymium binary / ternary complexes, such as nd ( acac ) 3 ' 2h2o, nd ( tfa ) 3 ' 2h2o, nd ( hfa ) 3 ' 2h2o, nd ( dbm ) 3 ' h2o, nd ( acac ) 3phen, nd ( tfa ) 3phen, nd ( hfa ) 3phen, nd ( dbm ) 3phen, nd ( tta ) 3 ( tppo ) 2, nd ( hfa ) 3 ( tppo ) 2, nd ( acac ) 4hpy, nd ( tta ) 4hpy and ndq3. the effects of organic ligands, synergistic coordination agents and different substitution groups for - diketones on effective line width and photoluminescence intensity of neodymium complexes were investigated. the photoluminescence spectra indicate that synergistic coordination agents can shield neodymium ion and impede water molecules penetrating into inner coordination shell to satisfy large coordination number of nd3 + during hydrous synthesis process, so the luminescence intensity of neodymium ternary complexes is stronger than that of neodymium binary complexes

    譜研究表明,由於協同試劑的參與,屏蔽了水分子參與配位,降低了羥基( oh )對釹離子激發態能級~ 4f _ ( 3 2 )的猝滅,三元配合物的熒光強度均比二元配合物,其中配合物nd ( tta ) _ 3 ( tppo ) _ 2在1340nm處的熒光強度,適合作為摻雜的學活性物質,來制備有源波導材料;在有水工藝條件下,單純地氟化配體未必能提高釹配合物的近紅外發性能。
  8. 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
  9. 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。
  10. 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。
  11. 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能量, pb離子的熒光強度明顯下降。
  12. 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;以染料rhodamineb為溫探針,建立了pdms微流控晶元上的溫-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色圖,對pdms微流控晶元的微流道溫特性進行了分析,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 。
  13. 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的濃及分佈變化,結果表明,分裂期細胞總體熒光強度于間期細胞;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主要集中於赤道板處;剛完成有絲分裂的細胞內則相對集中於兩端或其中的一端。
  14. 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,且促進其凋亡。
  15. 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 +具有很的絡合能力,而且在一定條件下它的熒光強度隨鈣離子濃增加而增
  16. 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,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。
  17. 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,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峰位置以及雙重熒光強度之間的比值不同。
  18. Based on the theoretical analysis and experimental researches, it is presented that the wider spectra are resulted from the many fluorophores with large numbers of vibrational energy levels on the ground level in the blood cells, and the reduction of the spectral intensity is due to the reabsorption of the blood cells and the energy transfer of the collisions between the fluorophore and another one or other macromolecule. on the other hand, when the concentration of the blood cells is increased, the reabsorption of the blood cells, the secondary fluorescence due to the reabsorption and the influence of the concentration on the energy levels of fluorophores are all the factors of the red - shifted spectral peaks

    在進行理論分析和研究的基礎上,提出了因血細胞中存在多種團,且這些團的電子能級上又存在大量的不同的振動能級,從而導致被激發的團發出較寬的譜;血細胞濃的增大,團以及其他大分子之間的距離變小,造成它們之間因碰撞的能量轉移概率加大,因而易產生猝滅,結果導致熒光強度的變小;血細胞溶液中重吸收所導致的猝滅和二次發射,以及血細胞濃的變化對其中團能級系統的影響都是導致峰值波長「紅移」的原因;進而研究了led誘導血細胞產生譜的機理。
  19. Aqueous fluid volume and [ c1 ~ j were assayed in samples withdrawn by micropipettes. intraocular pressure ( top ), pressure - dependent outflow, and anterior chamber compliance were determined from pressure measurements in response to pulsed and continuous fluid infusions into the anterior chamber using micropipettes. result : in wildtype mice ( gdi genetic background, age 4 - 6 weeks ), iop was 16. 0 ? 0. 4 mmhg, aqueous fluid volume was 7. 2 ? 0. 3 ul, aqueous fluid production was 3. 6 ? 0. 2 ul / hr, aqueous fluid outflow was 0. 36 ? 0. 06 ul / hr / mmhg, and anterior chamber compliance was 0. 036 ? 0. 006 ul / mmhg ( mean ? se, 8 - 10 eyes )

    實驗方法包括:將物質用電離子滲透的方法穿透角膜導入活體小鼠的前房中,然後應用共聚焦顯微鏡根據熒光強度變化測量房水生成率;通過顯微注射針吸取房水檢測房水容積和氯離子濃;顯微玻璃管刺入前房測量眼內壓,並將生理鹽水分別以連續和脈沖兩種方式注入前房,測量房水間隙的順應性和房水排出與眼內壓的相關性。
  20. To summarize, intense near uv, violent, blue, green, and red emitting can be obtained in si - based thin films through 0 and n doping

    綜上所述,通過氧、氮摻雜,在硅基薄膜中可獲得近紫外及紫、藍、綠和紅等波段的熒光強度取決于制備工藝方法及工藝參數。
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