Objective: To study the characterization of CK2 from HL 60 cells.
目的：研究人早幼粒白血病HL-60细胞蛋白激酶CK2的性质。
Objective:To search for natural substrates of protein kinase CK2 in pig platelets.
目的：寻找猪血小板中蛋白激酶CK2可能的天然底物。
CONCLUSION (Kaempferol is a) novel potent inhibitor of protein kinase CK2 in vitro.
结论山萘黄素是一种新的体外蛋白激酶CK2的有效抑制剂。
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 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。
CONCLUSIONS AG1109 not only was an effective inhibitor of protein tyrosine kinases, but also was a novel potent inhibitor of protein kinase CK2.
结论：AG110 9不仅是酪氨酸蛋白激酶的抑制剂，而且是一种十分有效的蛋白激酶CK2的抑制剂。
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。
Kinetic studies of AG114 inhibition on recombinant human CK2 showed that the inhibition was mixed competitive with GTP and noncompetitive with casein.
AG114对重组人ck2的动力学研究表明：它与GTP呈混合竞争性抑制作用，与酪蛋白呈非竞争性抑制作用。
The UL145 protein of the clinical strains were conserved and comprised phosphorylation motif sites for protein kinase C(PKC) and casein kinase 2(CK2).
所有先天感染患儿临床株的UL145编码蛋白具有蛋白激酶（C PKC）磷酸化功能位点和酪蛋白激酶（CK2）磷酸化功能位点。
Kinetic studies of AG1112 on recombinant human CK2 showed that the inhibition was mixed (competitive is dominant) with GTP and noncompetitive with casein.
AG 1112对重组人ck2的动力学研究表明：它与GTP和酪蛋白分别呈混合性和非竞争性抑制作用。
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。
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。
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 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。
应用推荐