原位杂交
免疫染色
细胞生物学
核糖核酸
生物
背景(考古学)
共焦显微镜
信使核糖核酸
共焦
荧光原位杂交
分子生物学
免疫组织化学
生物化学
基因
免疫学
数学
染色体
古生物学
几何学
摘要
Abstract Single molecule RNA fluorescence in situ hybridization (smFISH) has become the standard tool for high spatial resolution analysis of gene expression in the context of tissue organization. This article describes protocols to perform smFISH on whole‐mount mouse embryonic organs, where tissue organization can be compared to RNA expression by co‐immunostaining of known protein markers. An enzymatic labeling strategy is also introduced to produce low‐cost smFISH probes. Important considerations and practical guidelines for imaging smFISH samples using fluorescence confocal microscopy are described. Finally, a suite of custom‐written ImageJ macros is included with detailed instructions to enable semi‐automated smFISH image analysis of both 2D and 3D images. © 2018 by John Wiley & Sons, Inc.
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