您要查找的是不是:
- In weak acidic medium, sodium periodate can oxidize Coomassie brilliant blue G and cause discoloring of coomassie brilliant blue G, and manganese can catalyze this oxidizing reaction. 基于弱酸性条件下高碘酸钠能氧化考马斯亮蓝G褪色,锰对此褪色反应具有显著的催化作用,由此建立了催化高碘酸钠氧化考马斯亮蓝G褪色光度法测定痕量锰的新方法。
- Keywords Catalytic spectrophotmetry;Iron;Coomassie brilliant blue G; 催化反应;光度法;铁;考马斯亮蓝G;
- Catalytic Spectrophotometric Determination of Trace Manganese with Coomassie Brilliant Blue G 催化NaIO_4氧化考马斯亮蓝G褪色光度法测定痕量锰
- Determination of Trace Iron by Catalytic Spectrophotometry with Coomassie Brilliant Blue G 考马斯亮蓝G动力学光度法测定痕量铁的研究
- Keywords titanium;kinetic spectrophotometry;coomassie brilliant blue G;potassium bromate; 钛(;动力学光度法;考马斯亮蓝G;溴酸钾;
- coomassie brilliant blue G 考马斯亮蓝G
- Staining: with silver and coomassie brilliant blue staining. 染色:行银染和考马斯亮蓝染色;
- Un-adsorbed protein was detected by coomassie brilliant blue G-250 method. 用考马斯亮蓝G-250法检测未反应的蛋白质。
- The binding reaction of the dye coomassie brilliant blue with proteins have been studied. 研究了考马斯亮蓝与蛋白质的结合反应。
- The results were compared with traditional method(Coomassie Brilliant Blue R250). 并和考马斯亮蓝R250染色方法比较。
- Coomassie Brilliant Blue method was adopted to detect the protein content of seventeen kinds of allergens. 采用考马斯亮蓝G250检测17种变应原的蛋白质含量,与重量/体积法对照,发现按后者配制的变应原皮试液蛋白质含量悬殊。
- It involves the binding of Coomassie Brilliant blue to protein。However, detergents such as sodiu... 摘要:The bradford dye-binding assay is a colorimetric assay for measuring total protein concentration。
- Protein crystals, large or small, can be stained with Mercury bromphenol blue, Amido black 10B and Coomassie brilliant blue R250 or G250 but salt crystals are not. 本文报导了蛋白质晶体能被汞溴酚蓝、氨基黑10B和考马斯亮蓝R250或G250染色;而无机盐晶体不被染色.
- The purified GAD showed two main bands,67 kD and 44 kD,on SDS-PAGE by Coomassie Brilliant Blue R-250 and Western-Blot under reducing condition. 纯化的GAD在变性条件下电泳,经考马斯亮蓝R2 5 0染色以及Western Blot鉴定主要有两条带,分子量分别为6 7kD和4 4kD。
- In addition, the staining of mPEG with BaCla and la is more specific and sensitive than the Coomassie Brilliant Blue staining. SDS-PAGE采用BaCl_2和I_2对mPEG染色比考马斯亮蓝染色水蛭素更为灵敏,特异性也很高。
- The expressed protein yield reached 385mg/L in the 10L fermentor assayed by Coomassie brilliant blue stain G-250 method. 该条件用于指导小试(5L/10L罐),蛋白表达量达到了385mg/L;
- Then the gels were stained by Coomassie brilliant blue R-250,and analyzed using Image Master 2D Platinum v 5.0 software. 运用Image Master 2D Platinum v 5.;0凝胶图像分析软件对2-DE凝胶图像进行差异表达分析
- Method The Coomassie Brilliant Blue G250 was dissolved into the ethanol and phosphate,then the SDS-PAGE was stained with the solution. 方法用考马斯亮蓝G250和磷酸作为染色液,用水作为脱色液。
- Appearence, location and arrays of cortical microtubules are consistent with those of cellular network visualized by staining of Coomassie brilliant blue R250. 其出现时间、布状况以及排列形态,基本上与考马斯亮蓝染色法观察到的网状结构物相一致。
- The results of determination for three serum samples were identical with those obtained according to the Bradford method using Coomassie Brilliant Blue (CBB G-250). 本方法成功应用于三个血清样品中蛋白质总量的测定,其结果与考马斯亮蓝法(Coomassie Brilliant Blue,CBB G-250)测定结果一致。