• 欧兹坎用LED(发光二极管)作为光源,以此制造细胞的阴影。

    Ozcan USES an LED as his light source, creating cellular shadows.

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  • 这项技术的最初部分,是要构建一个能产生发光蛋白的细胞,这种发光蛋白最初从发光水母中获得。

    The technique starts by engineering a cell that can produce a light-emitting protein that was first obtained from glowing jellyfish.

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  • 梅特兰博士考虑,如果能使发光的蛋白质附着在病毒上,并控制它找到并感染癌细胞,就能很容易地看到肿瘤。

    Dr Maitland speculated that if he could attach glowing proteins to viruses programmed to find and infect cancer cells, he could make tumours easier to see.

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  • 这种感染不会损伤细胞,但是当病毒复制并感染新的癌细胞时,发光的蛋白质也会增多,从而使肿瘤变得越来越亮。

    The infection did not harm the cells, but as the virus replicated and infected new cancer cells, the glowing protein multiplied too. This caused the tumours to grow brighter and brighter.

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  • 这种感染不会损伤细胞,但是当病毒复制并感染新的癌细胞时,发光的蛋白质也会增多,从而使肿瘤变得越来越亮。

    The infection did not harm the cells, but as the virus replicated and infected new cancer cells, the glowing protein multiplied too.This caused the tumours to grow brighter and brighter.

    youdao

  • 免疫组化染色显示,发光组织中肿瘤细胞呈阳性。

    Immunochemistry demonstrated tumor cells were positive in the luminous tissues.

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  • 在一段持续的时间内,这些细胞每隔24个小时就发光一次。

    The cells emitted light once every 24 hours over a sustained period of time.

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  • 结果:ATP标准品浓度、K562细胞浓度的对数与荧光发光值的对数具极好的线性关系(P<0.001);

    Results: There is a wonderful linear relationship between the log concentration of ATP, K562 and log luminescent value (P< 0.001);

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  • 通过LED(发光二极管)光源,奥兹堪运用一种算法将由此产生的细胞阴影转换成细胞的图像。

    Ozcan USES an LED as his light source, creating cellular shadows. An algorithm turns those shadows into an image of the cells.

    youdao

  • 分别采用四氮唑蓝法和生物发光法测定各组大鼠血红细胞SOD活性及心肌at P含量。

    SOD activities in blood RBC and the myocardial ATP contents of rats in each group were determined respectively with NBT and bioluminescence methods.

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  • 结论不同浓度及不同培养时间的食管癌细胞其超微弱发光强度不同。

    ConclusionThe ultra-weak photon emission of esophageal cancer cells depends on their different concentrations and culture times.

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  • 目的研究肿瘤细胞不同浓度及不同培养时间与超微弱发光强度之间的关系。

    ObjectiveTo study the relation of different concentrations and culture time of esophageal cancer cells with their ultra-weak photon emission intensity.

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  • 感染本身于细胞无害,但由于病毒能够自我复制并感染新的癌细胞,所以发光蛋白也会成倍递增。

    The infection did not harm the cells, but as the virus replicated and infected new cancer cells, the glowing protein multiplied too.

    youdao

  • 科学家们在小白鼠大脑中标记出促食素细胞,使它们发光。然后在喂食小白鼠不同食物后,追踪这些细胞的活动。

    Scientists marked orexin cells in mice brains so they would fluoresce. Then they tracked the cells' activity after feeding the mice different kinds of food.

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  • 利用发光法灵敏的检测细胞毒性。

    Sensitive detection of cytotoxicity by luminescence method.

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  • 这些是荧光的色素细胞,它们在黑暗中像萤火虫一样发光。

    These are bioluminescent chromatophores, and they glow in the dark like fireflies.

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  • 面部清洁是促进细胞再生、令肌肤焕发光彩的最好时机。

    Cleansing your face is the perfect opportunity to encourage cell renewal for a brighter complexion.

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  • 用532nm的激光作为激发光源,分别测量正常人血液及血液组分(血浆、血小板、红细胞)的荧光光谱。

    A 532 nm laser was used as exciting source to measure the fluorescence spectra of human blood and its components (red blood cell, blood platelet and blood plasma).

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  • 另外,这些荧光蛋白基因还会随着癌细胞的复制而复制,因此这些癌细胞的后代也能发光。

    In addition, the gene for the glowing protein is passed on by the cancer cells as they replicate, so that their progeny glow too.

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  • 方法采用生物超微弱发光探测技术对食管癌细胞的超微弱发光进行研究。

    MethodsUltra-weak photon emission of esophageal cancer cells was detected using the biological ultra-weak emission detection techniques.

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  • 单色激发光源是单细胞荧光显微系统中的重要组成部分。

    Monochromator is a very important part in living cell fluorescence microscopy system.

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  • 单色激发光源是单细胞荧光显微系统中的重要组成部分。

    Monochromator is very important part in living cell fluorescence microscopy system.

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  • 超纯正常羊血清在发光和荧光免疫组化和免疫细胞化学方法中作为封闭液和抗体稀释液使用。

    Premium quality normal goat serum for use as blocking reagent and antibody diluent for chromogenic and fluorescent immunohistochemical and immunocytochemical assays.

    youdao

  • 超纯正常羊血清在发光和荧光免疫组化和免疫细胞化学方法中作为封闭液和抗体稀释液使用。

    Premium quality normal goat serum for use as blocking reagent and antibody diluent for chromogenic and fluorescent immunohistochemical and immunocytochemical assays.

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