(*contributed equally to this work) 发布: 2014年10月20日第4卷第20期 DOI: 10.21769/BioProtoc.1261 浏览次数: 14232
评审: Elias BassilRu ZhangAnonymous reviewer(s)
Abstract
The inflorescence stem of the flowering plant Arabidopsis thaliana (thale cress) is an excellent model system to investigate plant vascular tissue patterning and development. Plant vasculature is a complex conducting tissue arranged in strands called vascular bundles, formed by xylem (tissue that carries water) and phloem (tissue that carries photosynthates and signaling molecules). Xylem and phloem are originated from cell division of the meristematic cells of the vascular cambium. In Arabidopsis the flowering stem elongates about three weeks after germination. At this stage it is possible to visualize defects in its development and morphology. Here we describe a protocol to embed in plastic (resin) stem segments either freshly dissected from living plants or previously assayed for β-glucuronidase. This protocol provides an excellent cellular morphology ideal to visualize stem cell types including those of vascular bundles using high-resolution light microscopy.
Keywords: Arabidopsis (拟南芥)Materials and Reagents
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文章信息
版权信息
© 2014 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Chevalier, F., Iglesias, S. M., Sánchez, Ó. J., Montoliu, L. and Cubas, P. (2014). Plastic Embedding of Arabidopsis Stem Sections. Bio-protocol 4(20): e1261. DOI: 10.21769/BioProtoc.1261.
分类
植物科学 > 植物细胞生物学 > 细胞成像
植物科学 > 植物发育生物学 > 形态建成
细胞生物学 > 细胞成像 > 固定组织成像
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