Protein kinase assay was used to detect the activity of MKK6 in cells.
使用激酶活性测定法检测细胞内mkk6的激酶活性。
ERK activity was measured by ERK1/2 immuno-precipitation kinase assay kit;
免疫沉淀法纯化蛋白并用ERK1/2试剂盒测定ERK活性；
Kinase Buffer can be used to assay protein kinase activity.
激酶缓冲液用来分析蛋白激酶的活性。
The assay begins with a standard kinase reaction performed in the provided reaction Buffer with a provided Bisamide Rhodamine 110 peptide substrate (PKA R110 substrate).
检测开始时、先用试剂盒提供的PKA双酰胺罗丹明110肽底物进行一个标准的激酶反应。
The phosphorylation assay proves that aldose reductase is the substrate of insulin-receptor tyrosine kinase and the Tyr(40) and Tyr(49) are phosphorylated by the kinase.
在试管内，未磷酸化的醛糖还原酶和磷酸化的醛糖还原酶的动力学常数无差异，而细胞内的情况有待于进一步研究。
The phosphorylation assay proves that aldose reductase is the substrate of insulin-receptor tyrosine kinase and the Tyr(40) and Tyr(49) are phosphorylated by the kinase.
在试管内，未磷酸化的醛糖还原酶和磷酸化的醛糖还原酶的动力学常数无差异，而细胞内的情况有待于进一步研究。
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