Coomassie Brilliant Blue method was used to quantify the proteins in cells.
考马斯亮蓝微板法测定细胞内蛋白总量。
The results were compared with traditional method (Coomassie Brilliant Blue R250).
并和考马斯亮蓝r 250染色方法比较。
Then the total protein content was measured by using Coomassie brilliant blue staining.
考马斯亮蓝法测定人牙周膜细胞的总蛋白含量。
The content of proteins in Xinjiang wild hops was determined by the dying method with coomassie brilliant blue.
采用考马斯亮蓝染色法对新疆野生啤酒花中水溶性蛋白质含量进行测定。
However, with Coomassie brilliant blue method and other new detection method, Lori citations gradually decline curve.
不过，随着考马斯亮蓝法等新检测方法的出现，洛瑞论文的引用曲线渐渐下滑。
The paraformaldehyde prefixed-coomassie brilliant blue staining is a convenient cytoskeleton staining method for muscle cell.
为了观察肌细胞骨架，对传统考马斯亮蓝染色法进行改良，并与免疫荧光染色法进行了比较。
The paraformaldehyde prefixed-coomassie brilliant blue staining is a convenient cytoskeleton staining method for muscle cell…
因此，多聚甲醛预固定-考马斯亮蓝染色法是一种适于肌细胞骨架染色的简便方法。
Myocardial mitochondria was extracted by differential centrifugation, and protein level was measured by Coomassie brilliant blue method.
用差速离心法提取心肌线粒体，考马斯亮蓝法测定蛋白含量。
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.
用pH3 -10的IPG胶条进行双向电泳，经考马斯亮蓝染色后，可在胶面上检测到大约450个蛋白点，其中约有89%的蛋白是酸性蛋白。
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是蛋白质分析、比较和特性鉴定的有效方法，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。
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.
用蒽酮比色法和酚硫酸法测定产品糖含量，考马斯亮蓝法测定蛋白质含量。
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.
用改良的考马斯亮蓝法对硅片和改性后的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在改性前后硅表面的黏附行为。
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.
用改良的考马斯亮蓝法对硅片和改性后的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在改性前后硅表面的黏附行为。
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