Section in situ hybridization using either radioactive or nonradioactive labeled cDNA probes is an invaluable technique that enables the investigator to detect and localize mRNA expression within tissue sections and cells. Here, we describe the labeling of 35 S-UTP radioactive and nonradioactive digoxigenin probes, preparation of tissue sections, hybridization, and washing of non-hybridized probes, followed by the detection of radioactive signals via dipping in nuclear emulsion and the immunohistochemical and subsequent colorimetric detection of nonradioactive signals. © Springer Science+Business Media New York 2014.
CITATION STYLE
Simmons, O., Bolanis, E. M., Wang, J., & Conway, S. J. (2014). In situ hybridization (Both Radioactive and Nonradioactive) and spatiotemporal gene expression analysis. Methods in Molecular Biology, 1194, 225–244. https://doi.org/10.1007/978-1-4939-1215-5_12
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