RNA transcripts are a critical piece of the central dogma of biology yet are difficult to image due to their requirement for specific, fluorescent labeling and nanoscopic size. Bruker’s Vutara single-molecule localization microscope (SMLM) and fully integrated SRX software enables users to easily conduct smFISH imaging and analysis experiments.
Bruker offers the tools necessary for successful smFISH and super-resolution experiments including our:
Single molecule fluorescence in situ hybridization (smFISH) — also known as smRNA FISH or RNA FISH — is a cutting-edge technique for studying gene expression in single cells. This technique is similar to FISH in that it is used to visualize DNA, either specific genes or portions of genes, but differs in its unique ability to image and quantify individual RNA molecules. The applications of smFISH transcend life sciences disciplines and include, among others, genomics, cancer biology, neuroscience, and more.
Performing smFISH experiments with the Vutara not only allows for quantification of RNA, but also enables the visualization of the target RNA at subcellular resolution. The ability to image the RNA within the cell opens avenues to studying RNA distribution and localization in relation to other markers or proteins. The combination of the imaging and quantification with smFISH can also be used as a readout for prediction of protein content. The advantage of RNA imaging with smFISH with the Vutara is unique from RNA sequencing data, which only provides quantitative values of RNA abundance.
RNA imaging with smFISH enables quantitative and qualitative gene expression experiments within single cells. With smFISH, researchers can measure cellular mRNA and perform spatial localization and quantification in locations such as the cytoplasm and nucleus. Single RNA molecules can be traced over time for temporal analysis.
Single-molecule fluorescence in situ hybridization (smFISH) enables the visualization and quantification of RNA molecules at single-molecule resolution. This is achieved by hybridizing many short, fluorescently-labeled oligonucleotide probes to specific RNA targets. The technique is typically performed on fixed cells to ensure high specificity and spatial resolution.