Conclusion Genistein and daidzein were two effective inhibitors of recombinant human protein kinase CK2 in vitro.
结论染料木黄酮和大豆甙元是两种有效的重组人CK2全酶的抑制剂。
AIM: to observe the inhibitory effect of luteolin on recombinant human protein kinase CK2 holoenzyme and to confirm the inhibitory type by its enzyme kinetic analysis in vitro.
目的：观察体外藤黄菌素对重组人蛋白激酶CK2的抑制效果及进行酶动力学分析以确定其抑制作用类型。
AIM To study the effects and kinetics of sodium quercetin 7 sulphate (SQMS) on recombinant human protein kinase CK2 holoenzyme.
目的观察槲皮素7硫酸酯钠盐(SQMS)对重组人CK2全酶的直接作用及酶动力学机制。
This study was to search specific CK2 inhibitors in tumor cells through observation of the inhibitory effects of baicalein on recombinant human protein kinase CK2 holoenzyme and its kinetics in vitro.
为了寻找肿瘤细胞内ck2的特异性抑制剂，本研究观察黄芩甙体外对重组人蛋白激酶CK2的抑制效果，并进行酶动力学分析以确定其抑制作用类型。
This study was to search specific CK2 inhibitors in tumor cells through observation of the inhibitory effects of baicalein on recombinant human protein kinase CK2 holoenzyme and its kinetic.
为了寻找肿瘤细胞内ck2的特异性抑制剂，本研究观察黄芩甙体外对重组人蛋白激酶CK2的抑制效果，并进行酶动力学分析以确定其抑制作用类型。
The recombinant human protein kinase CK2 may be used as a molecular target for simpler screening and development of more effective inhibitors of CK2.
重组人蛋白激酶CK2可作为一种较为简便筛选和开发有效的CK 2抑制剂的分子靶点。
The recombinant human protein kinase CK2 may be used as a molecular target for simpler screening and development of more effective inhibitors of CK2.
重组人蛋白激酶CK2可作为一种较为简便筛选和开发有效的CK 2抑制剂的分子靶点。
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