发布: 2012年12月20日第2卷第24期 DOI: 10.21769/BioProtoc.309 浏览次数: 21904
Abstract
The production of hydrogen peroxide (H2O2) has been recognized as an important feature of plant cells that undergo programmed cell death (PCD) during host-pathogen interaction. Thordal-Christensen et al. (1997) first described a method using chemical 3,3-diaminobenzidine (DAB) to detect the presence and distribution of H2O2 in barley leaves challenged by the powdery mildew fungus (Thordal-Christensen et al., 1997). Since then, this method has been adapted to many other plant species for in situ detection of H2O2. Here, we describe a modified protocol to stain and visualize H2O2 production in wheat leaves during infection by the necrotrophic fungus, Stagonospora nodrum or infiltration by the necrotrophic effectors produced by the fungus. The short version of this method has been reported in (Liu et al. 2012).
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版权信息
© 2012 The Authors; exclusive licensee Bio-protocol LLC.
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分类
植物科学 > 植物细胞生物学 > 组织分析
细胞生物学 > 细胞染色 > 活性氧
生物化学 > 其它化合物 > 活性氧
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