• Coomassie Brilliant Blue method was used to quantify the proteins in cells.

    马斯亮微板测定细胞内蛋白总量。

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  • The results were compared with traditional method (Coomassie Brilliant Blue R250).

    考马斯亮r 250染色方法比较

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  • Then the total protein content was measured by using Coomassie brilliant blue staining.

    马斯亮测定人牙周膜细胞的蛋白含量

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  • The content of proteins in Xinjiang wild hops was determined by the dying method with coomassie brilliant blue.

    采用考马斯亮染色对新疆野生啤酒花水溶性蛋白质含量进行测定

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  • However, with Coomassie brilliant blue method and other new detection method, Lori citations gradually decline curve.

    不过随着马斯亮检测方法的出现,洛瑞论文的引用曲线渐渐下滑

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  • The paraformaldehyde prefixed-coomassie brilliant blue staining is a convenient cytoskeleton staining method for muscle cell.

    为了观察细胞骨架,对传统考马斯亮染色进行改良,并与免疫荧光染色法进行了比较。

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  • The paraformaldehyde prefixed-coomassie brilliant blue staining is a convenient cytoskeleton staining method for muscle cell

    因此,多聚甲醛固定-考马斯亮染色一种适于细胞骨架染色的简便方法

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  • Myocardial mitochondria was extracted by differential centrifugation, and protein level was measured by Coomassie brilliant blue method.

    速离心法提取心肌线粒体,考马斯亮测定蛋白含量。

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  • Stained with coomassie brilliant blue, nearly 450 protein spots in a 2-de gel were detected with the pH 3 ~ 10 gradient IPG strip, among which about 89% proteins were acidic ones.

    pH3 -10IPG胶条进行双向电泳,考马斯亮染色后,可面上检测大约450个蛋白其中约有89%的蛋白是酸性蛋白。

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  • PAGE is an effective method for the analysis, comparison and identification of protein. The removal of the coomassie brilliant blue (CBB) from the gel is generally inefficient in SDS_PAGE.

    PAGE蛋白质分析比较特性鉴定有效方法,常规SDS -PAGE分析蛋白过程中考马斯亮蓝色素脱除过程耗时低效。

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  • The reactions of saccharide with Anthron and phenol_sulphate acid are used to analyze saccharide content. The content of protein in the products is determined by Coomassie Brilliant Blue method.

    蒽酮比色硫酸测定产品含量考马斯亮测定蛋白质含量。

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  • The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.

    改良马斯亮硅片改性后硅片进行了蛋白质吸附研究,并采用荧光显微镜观察了胎鼠海马神经细胞改性前后硅表面黏附行为

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  • The amount of adsorbed protein on original and modified silicon surfaces was measured by a Coomassie brilliant blue protein assay. Cell adhesion behavior was then assessed by fluorescence microscopy.

    改良马斯亮硅片改性后硅片进行了蛋白质吸附研究,并采用荧光显微镜观察了胎鼠海马神经细胞改性前后硅表面黏附行为

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