熒光特性波長 的英文怎麼說

中文拼音 [yíngguāngxìngzhǎng]
熒光特性波長 英文
characteristic fluorescent wavelength
  • : 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) ...
  • : Ⅰ形容詞(特殊; 超出一般) particular; special; exceptional; unusual Ⅱ副詞1 (特別) especially; v...
  • : Ⅰ名詞1 (性格) nature; character; disposition 2 (性能; 性質) property; quality 3 (性別) sex ...
  • : Ⅰ名詞1 (波浪) wave 2 [物理學] (振動傳播的過程) wave 3 (意外變化) an unexpected turn of even...
  • : 長Ⅰ形容詞1 (年紀較大) older; elder; senior 2 (排行最大) eldest; oldest Ⅱ名詞(領導人) chief;...
  • 特性 : characteristic(s); character; performance; features; properties; behaviour; response; character...
  • 波長 : [物理學] wavelength波長標準 [光學] wavelength standards; 波長測量 wavelength measurement; 波長常...
  1. Fluo - 3, a visible light - excitable ca2 + indicator, overcomes the limitation of quin - 2, indo - 1 and fura - 2 but no longer display any spectral shifts upon ca2 + binding and thus rati ometric measurements are not possible

    表明所合成試劑stdin ? am是目前國內外唯一的可以am酯型無損傷導入細胞、雙、可見激發的胞漿ca ~ ( 2 + )探針。
  2. 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學成像理論,討論了不同對單子和雙子共焦顯微鏡成像的影響,導出了單子和雙子共焦顯微鏡的功率傳輸函數、三維脈沖響應函數和三維學傳遞函數,得到了它們在不同激發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,當激發的比值下降到一定程度時,可以看到不同程度的失錐現象。
  3. Because of the nonlinear effect, the imaging property of two - photon confocal microscopy is very different from that of the conventional confocal microscopy. that the fluorescent wavelength equals to the excitation wavelength has been discussed theoretically as we know

    在僅有的理論研究中,絕大多數文獻都只是討論了等於激發這一殊情況,很少討論不同對共焦顯微鏡成像的影響。
  4. 2. confocal microfluoroscope and the new fluorescent ca2 + indicator stdin - am were used to investigate the mechanism of 5 - hydroxytryptamino ( 5 - ht ) on intracellular calcium dynamics in cultured rat stomach fundus smooth muscle cells comparing with that of fluo - 3. the results shown that the new fluorescent ca2 + indicator, stdin, developed in our laboratory

    結果表明,所合成試劑既具備雙探針f盯a一2與c擴+結合前後吸收和峰位移,又保持了探針fluo一3激發位於可見區的
  5. The indicators quin - 2, indo - land fura - 2 have the advantage of wavelength - shift upon binding ca2 + but share a common drawback in that the excitation bands for these indicators occur at uv wavelength ( 340 - 360nm ), where autofluorescence from cells is high, radiation - damage of cellular structures is serious, the transmission of microscope optics is poor, and the availability of aberration - corrected optics for confocal microscopy is limited

    迄今為止,尚未見既可激發、又與ca ~ ( 2 + )結合后峰位移、且對胞內ca ~ ( 2 + )測定具、可在亞細胞水平進行ca ~ ( 2 + )測定的整體能優良的鈣探針及其在生命科學中的應用研究報道。
  6. Then we grew the material with different active layer growth temperature, different v / ratio, different doping concentration and form. after that, we tested these materials by photoluminescence ( pl ) technology, and got the best growth condition according to the results of photoluminescence spectra. our result was that the active layer growth temperature was 700, v / ratio was 60, waveguide layer doping was gradual changed ( n - type doping with sih4 from 190sccm to 590sccm, p - type doping with dmzn from 90sccm to 490sccm )

    然後在不同的有源區生溫度、 /比、摻雜方式及濃度情況下對激器材料進行外延生,並利用( pl )技術對不同生條件下外延材料的致發進行了測試對比,結果表明在下列條件下生出來的材料具有更好的學和電學能:有源區生溫度在700 、導層/比選擇為60 、 n型導漸變摻雜190sccm - 590sccm的sih _ 4 、 p型導漸變摻雜90sccm - 490sccm的dmzn 。
  7. Not only can it be excited by visible light but also displays a spectrum - shift upon binding with ca +. moreover, it targets precisely into cytosol only, and thereby exhibits great advantage beyond flou - 3 and ruro - 2. thus it is possible to use stdin - am to measure real - time variation of [ ca2 + ] in cytosol

    同時細胞圖像分析顯示, stdhi一am進入細胞后只標記胞漿c擴+而不標記胞核c擴+ ,是目前唯一的可以am酉旨型無損傷導入細胞、雙、可見激發的胞漿c擴+探針。
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