2) DNA-photocleavage agents
DNA切割剂
3) DNA cleavage
DNA切割
1.
Determining the base sequence of DNA broken site is quite crucial for the study on the cleavage site specificity and mechanism of various natural or synthetic DNA cleavage regents,and on developing novel therapeutic drugs targeting at DNA.
定向设计、开发具有特定识别和切割序列的DNA切割试剂(限制性内切酶、金属核酸酶等)在生物技术领域中具有广阔的应用前景[1~4]。
2.
The kinetics of DNA cleavage,especially the conversion of supercoiled to nicked DNA,by two 4,4′-dimethyl-2,2′-pyridyl(dmbpy) manganese(Ⅱ) complexes,Mn(dmbpy)2(OCN)2(1) and Mn(dmbpy)2(dca)2(2),was investigated.
对2个4,4′-二甲基-2,2′-联吡啶锰(Ⅱ)配合物在生理条件及H2O2的存在下对DNA切割的动力学进行了研究。
3.
The results showed that the complexes had the ability of interaction with DNA and DNA cleavage.
结果表明这2个配合物能与DNA发生作用,并具备DNA切割能力。
5) nickasse
(DNA)切口酶
6) DNA shear
DNA 切变
补充资料：DNA分子花窗(沿B―DNA轴线方向看)
[图]
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条