摘要
为了研究小麦转录因子基因TaMyb2-Ⅱ的功能,利用SalⅠ和SacⅠ双酶切的方法,构建了基因克隆及表达载体PEBV,获得了正义PEBV-35Sp-TaMyb2-Ⅱ-NOSter阳性克隆,实现了TaMyb2-Ⅱ基因的定向克隆。
In order to analyse the function of wheat TaMyb2- Ⅱ gene, clone and expression vector PEBV was constructed and sense PEBV-35Sp-TaMyb2-NOSter positive clone was obtained by Sal Ⅰ and Sac Ⅰ double digests. Thus the TaMyb2- Ⅱ was directional cloned.
出处
《山西农业大学学报(自然科学版)》
CAS
2009年第2期104-105,共2页
Journal of Shanxi Agricultural University(Natural Science Edition)
基金
山西省青年科技研究基金(2008021044)
山西农大科技创新基金(2006024)
山西农大博士科研启动金(412549)