Coiro Mario, Truernit Elisabeth
Department of Biology, ETH Zurich, Universitätsstrasse 2, 8092, Zürich, Switzerland.
Department of Systematic and Evolutionary Botany, University of Zurich, Zollikerstrasse 107, 8008, Zürich, Switzerland.
Methods Mol Biol. 2017;1544:127-132. doi: 10.1007/978-1-4939-6722-3_11.
An improved pseudo-Schiff propidium iodide staining technique well suited for, but not limited to, the visualization of xylem cell walls in whole mount samples is presented. The pseudo-Schiff reaction results in covalent binding of the fluorescent dye propidium iodide to cell walls. This stable linkage permits the use of clearing agents after staining, which is itself improved following pretreatment of the plant tissue. A subsequent acid alcohol washing step eliminates unbound propidium iodide to reduce background fluorescence. The method can be used for characterizing xylem cell structure in different organs and species without the need for tissue sectioning.
本文介绍了一种改进的伪席夫碘化丙啶染色技术,该技术非常适合但不限于对整装样本中的木质部细胞壁进行可视化观察。伪席夫反应使荧光染料碘化丙啶与细胞壁发生共价结合。这种稳定的连接允许在染色后使用透明剂,而在对植物组织进行预处理后,透明剂本身也得到了改进。随后的酸醇洗涤步骤可去除未结合的碘化丙啶,以减少背景荧光。该方法可用于表征不同器官和物种中的木质部细胞结构,而无需进行组织切片。