克莱诺碎片
DNA聚合酶Ⅰ
DNA聚合酶
核酸外切酶
底漆(化妆品)
化学
片段(逻辑)
DNA
聚合酶
基质(水族馆)
模板
分子生物学
组合化学
聚合酶链反应
生物化学
生物
逆转录酶
纳米技术
材料科学
程序设计语言
计算机科学
有机化学
生态学
基因
作者
Tian Tian,Shuang Peng,Heng Xiao,Yuelin Long,Boshi Fu,Xiaoe Zhang,Shan Guo,Shaoru Wang,Xiang Zhou,Song‐Mei Liu,Xin Zhou
摘要
Here, we first demonstrated that 5-MedCTP could be incorporated into the synthetic DNA template by the exonuclease deficient Klenow fragment with a much higher efficiency than dCTP and 5-hydroxymethyl-dCTP. Further, we first conducted a comparable study of primer extension reaction using templates containing deoxycytidine (dC) or 5-methyldeoxycytidine (5-mdC) for incorporating different triphosphates. Based on our findings, 5-methyldeoxycytidine could enhance the substrate activity of the Klenow fragment (exo-) and this feature could potentially be used in DNA methylation analysis.
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