熒光測定計 的英文怎麼說

中文拼音 [yíngguāngcèdìngjì]
熒光測定計 英文
photofluorometer
  • 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） ...
  • 測 : 動詞1. （測量） survey; fathom; measure 2. （測度; 推測） conjecture; infer
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 計 : Ⅰ動詞1 （計算） count; compute; calculate; number 2 （設想; 打算） plan; plot Ⅱ名詞1 （測量或計算...
  • 測定 : determine; determination; setting-out; admeasurement; assignment; assay; finding
  1. After study on the technology of probe head of the optical fiber, a biosensor for determination of cholesterol which based on fluorescence quenching and adopted phase shift & phase lock technique to detect the change of light intensity was developed, in this biosensor, the cellulose acetate cod enzyme membrane was took as sensitivity basic dollar, ru ( phen ) 32 + was took as indicator of oxygen and furcated optical fiber as conduct carrier of light signal

    通過對光纖探頭組裝技術的研究，以醋酸纖維素cod酶膜為敏感基元，釕（ ） -鄰菲咯啉為氧指示劑，分叉光纖為光信號傳導載體，採用相移法和鎖相放大技術設計了一種基於熒光猝滅原理的測定膽固醇用的生物傳感裝置。
  2. 7. at the first time, the reporter dye, fam was linked to the 5 " - end of the oligonucleotides of the probes, and the tamra was located at the 3 " - end as quencher dye. we use camv35s and fmv promoter, nos terminater, mark gene nptii, and aim gene pat, epsps and cryla ( b ) genes as target sequences, design pairs of sp

    7 、首次以fam熒光素標記探針5 』端作為發光基團，以tarma標記探針3 』端為淬滅基團，以camv35s 、 fmv啟動子、 nos終止子、標記基因nptll 、抗除草劑基因epsps 、 pat 、抗蟲基因cry1a ）為檢狽目標，設計、篩選出特異性引物和探針，優化實驗參數，建立了轉基因植物通用性熒光pcr定性檢測方法體系。
  3. On the basis of the mentioned above and the real - time pcr principal, we have designed and optimized the primers and probes, set up the real - time qualitative pcr detection system. meanwhile, using the endogenous zein - maize and lectin - soybean as interior collate gene, epsps and cryia ( b ) as target genes, set up the real - time quantitative pcr detection system

    在此基礎上，根據熒光pcr原理，設計、優化引物和熒光探針，建立了熒光pcr定性檢測方法體系，並以玉米內源基因（ zein ） 、大豆內源基因（ lectin ）作為內標基因，以epsps和cryia （ b ）作為目的基因，建立了熒光pcr定量檢測方法體系。
  4. Milk and milk products - determination of alkaline phosphatase activity - fluorimetric method for milk and milk - based drinks

    奶和奶製品.堿性磷酸酶活性的測定.牛奶和牛奶飲料的熒光計法
  5. Milk and milk products - determination of alkaline phosphatase activity using a fluorimetric method - fluorometric method for cheese

    奶和奶製品.用熒光計法測定堿性磷酸酶的活性.乳酪的熒光計法
  6. The pl spectra of the ag - sio2 composite films have been obtained from the fluorophotometer

    採用熒光光度計測定了ag - sio _ 2納米復合薄膜的光致發光性能。
  7. Part i this paper has minutely studied the interaction between ag ( i ) and serum albumin. the binding of ag ( i ) to human serum albumin ( hsa ) or bovine serum albumin ( bsa ) has been studied by equilibrium dialysis at ph ( 5. 4 ). the scatchard analysis indicates that there exists several strong binding sites of ag ( i ) in both hsa and bsa. a notable hysteretic effect has been observed in the interaction of ag ( i ) with hsa or bsa using uv - visible spectrometry at ph ( 5. 4 ), which shows that the binding between ag ( i ) with hsa or bsa may induce a slow transition of hsa or bsa from the conformation of weaker affinity for ag ( i ) to one of stronger affinity ( a - b transition ). the rate constants and activation parameters of this transition parameters of this tansition were measured and discussed. the binding equilibrium has been also studied by resonance light - scattering spectrum ( rls ) and flurescence quenching

    第一部分：等離子點ph （ 5 . 4 ）條件下，用平衡透析法和紫外光譜，熒光光譜，共振散射光譜研究了ag （ ）與人血清白蛋白（ humanserumalbumin ，簡稱hsa ）或牛血清白蛋白（ bovineserumalbumin ，簡稱bsa ）的結合。 scatchard圖分析表明， ag （ ）在hsa或bsa中有強弱兩類結合部位，通過計算機擬合獲得結合的逐級穩定常數值。紫外掃描發現ag （ ）與hsa或bsa的結合存在滯後效應，表明ag （ ）與hsa或bsa的結合可能誘導蛋白質構象發生緩慢變化（ a - b ） ，測得並討論了這一構象變化的速度常數和活化參數。
  8. In this work, according to the feature of soft x - ray fluorescence, a setup has been established for the measurement of soft x - ray fluorescence in laboratory, which is calibrated by 55fe. the setup is made of x - ray tube, fine tuning table, vacuum system, gas - flow proportional counter and multiple channel analysis

    本文工作中依據軟x射線熒光的特點，在實驗室建立了一套軟x射線熒光測量裝置，該裝置由x射線管、精密微調樣品臺、真空系統和流氣正比計數管探測系統以及多道分析儀組成，並採用~ （ 55 ） fe標準光源對系統進行實際標定。
  9. According to the gene sequence and secondary structure of hcv ns5b, we design the sirnas targeting ns5b gene following with the requirement for sirnas design from tuschl et. al and synthesize it from dharmacon company ; hepg2 cell stably expressing ns5b - egfp protein was trasfected by synthesized sirnas with electroportion, the non - transfected cell and non - specific sirnas transfected cell are c onsidered as control group ; inhibitory effect of sirnas was investigated by fluorescence microscope with dapi dyeing and by semi - quantitative rt - pcr

    然後根據dsrna設計原則，結合nssb基因的序列特徵，藉助生物信息學軟體設計了針對nssb基因的sirnas ，並交由公司化學合成；電穿孔法轉染上述穩定轉染的細胞克隆，同時分別以非特異的sirnas轉染組和空白轉染組為對照， dapi染色后通過熒光顯微鏡和內標化rtpcr檢測，初步證實了化學合成的sirnas可以特異阻斷nssb基因的表達。
  10. The phase structure of different cu - fe thin films were studied by using grazing incidence x - ray analysis ( gixa ). the texture and residual stress of different cu - fe thin films were measured by scan of x - ray diffraction ( xrd ) and 2 scan with different. the thicknesses of different thin films were characterized by means of small angle x - ray scattering ( saxs ) technique. by using atomic force microscope ( afm ) measured surface roughness of thin films. the component of different thin film was characterized by energy disperse spectrum ( eds ) and x - ray fluorescence ( xrf ). the magnetic properties of cu - fe thin films were measured by means of vibrating sample magnetometer ( vsm ). in addition, the giant magnetoresistance ( gmr ) effects of different films were also measured. the original resistance of the film fabricated by a direction - current magnetron sputtering system is directly affected by bias voltage

    利用掠入射x射線分析（ gixa ）技術對不同cu - fe薄膜的相結構進行了研究;利用xrd掃描及不同角度的2掃描對薄膜進行了結晶織構及殘余應力分析;運用小角x射線散射（ saxs ）技術測量了薄膜的厚度;採用原子力顯微鏡（ afm ）觀察了薄膜的表面形貌;運用能量損失譜（ eds ）及x射線熒光光譜（ xrf ）對薄膜進行了成分標定;使用振動樣品磁強計測量了不同cu - fe過飽和固溶體薄膜的磁性能;最後利用自製的磁阻性能測試設備測量了真空磁場熱處理前後不同薄膜的巨磁阻值。
  11. Milk and milk products - determination of alkaline phosphatase activity - part 2 : fluorometric method for cheese

    牛奶和奶製品.堿性磷酸酶活性的測定.第2部分:乾酪的熒光計法
  12. A series of validation experiments and genetic studies should be performed for the y - str multiplex system according to the suggestion of the technical work group dna analysis methods ( twgdam ). method we selected four y - str loci, dys434, dys438, dys439, a10 ( y - gata - a10 ) and designed two set of tailed primers to improve the efficiency of the multiplex pcr

    方法選定四個y染色體str基因座，應用加尾序列引物設計策略設計的引物，構建四個基因座的y - str復合擴增體系，建立銀染檢測和熒光檢測方法，依據dna分析技術工作組（ twgdam ）指南進行法醫學可行性研究和群體遺傳研究。
  13. Chapter 2 in the design of sensors and switches based on photoinduced electron transfer, fluorescence was often used with high sensitivity and convenience. it is noteworthy that room temperature phosphorescence ( rtf ) has many advantages over fluorescence, e. g., large stokes shift, higher signal to noise ratio, good selectivity and easily measurable luminescence lifetimes etc., and it can be found as a helpful complementary method of fluorescence sensing

    第二章在光誘導電子轉移傳感器和分子開關的設計中，熒光由於其靈敏度高、使用方便，受到人們的廣泛關注，相對于熒光室溫磷光選擇性好、信噪比高、較大的stokes位移、壽命易測定等優點，在許多方面與熒光互補。
  14. A simulation method is proposed to predict the motion artifacts of plasma display panels ( pdps ). the method simulates the behavior of the human vision system when perceiving moving objects. the simulation is based on the measured temporal light properties of the display for each gray level and each phosphor. both the effect of subfield arrangement and phosphor decay are involved. a novel algorithm is proposed to improve the calculation speed. the simulation model manages to predict the appearance of the motion image perceived by a human with a still image. the results are validated by a set of perceptual evaluation experiments. this rapid and accurate prediction of motion artifacts enables objective characterization of the pdp performance in this aspect

    針對目前等離子顯示屏普遍存在的運動偽像問題，提出了一種新穎的模擬計算方法，該方法實現了對等離子體顯示屏運動偽像的準確、快速估計.該方法通過測量等離子顯示屏不同顏色不同灰度下光信號隨時間的變化情況，模擬人眼對運動圖像的視覺感知行為，模擬計算出任意圖像以一定速度運動下的視覺感知效果.新演算法不但加入了等離子顯示屏熒光粉的延遲效應的影響，而且提高了模擬計算速度.所得模擬結果與實際主觀視覺感知實驗相符.這種快速準確的估計使對等離子顯示器件運動偽像的客觀評價成為可能
  15. Abstract : a simulation method is proposed to predict the motion artifacts of plasma display panels ( pdps ). the method simulates the behavior of the human vision system when perceiving moving objects. the simulation is based on the measured temporal light properties of the display for each gray level and each phosphor. both the effect of subfield arrangement and phosphor decay are involved. a novel algorithm is proposed to improve the calculation speed. the simulation model manages to predict the appearance of the motion image perceived by a human with a still image. the results are validated by a set of perceptual evaluation experiments. this rapid and accurate prediction of motion artifacts enables objective characterization of the pdp performance in this aspect

    文摘:針對目前等離子顯示屏普遍存在的運動偽像問題，提出了一種新穎的模擬計算方法，該方法實現了對等離子體顯示屏運動偽像的準確、快速估計.該方法通過測量等離子顯示屏不同顏色不同灰度下光信號隨時間的變化情況，模擬人眼對運動圖像的視覺感知行為，模擬計算出任意圖像以一定速度運動下的視覺感知效果.新演算法不但加入了等離子顯示屏熒光粉的延遲效應的影響，而且提高了模擬計算速度.所得模擬結果與實際主觀視覺感知實驗相符.這種快速準確的估計使對等離子顯示器件運動偽像的客觀評價成為可能
  16. Blood. determination of zinc protoporphyrin. hematofluorometer method

    血中鋅原卟啉的血液熒光計測定方法
  17. Leaf disks from tobacco are infected with cultures of a. tumefaciens transconjugants harboring the different plasmids, and transgenic plants are generated by the leaf disk procedure, plant extracts are analyzed by the fluorescent method for detecting gus activity. conclusions are drawn from our experiments and shown below : 1

    融合啟動子與gus報告基因融合構建相應的植物表達載體，並以含camv35s啟動子的表達載體pbi121作對照轉化煙草nc89 ，利用熒光分光光度計法定量測定各轉基因煙草植株的gus基因表達活性。
  18. A novel real - time fluorescent rt - pcr was established to detect pnrsv this technique uses a taqman probe to monitor in real time amplification of target genes, a taqman probe labeled by a quenching and fluorecenting was added to the pcr reaction buffer

    另外還設計了taqman熒光探針，確定了檢測條件和參數，建立了實時熒光rtwcr方法，該方法是指在pcr反應體系中加入帶有熒光基團互補探針，如果有pcr反應（擴增） ，熒光信號就較大。
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