Multiplexing immunofluorescence imaging enables the analysis of the whole tissue microenvironment: the single cell resolution combined with spatial localization retrieves the information of cellular relationships and organization within the same morphological context. However, the complexity of the analysis, time-consuming optimization, and significant challenges in results reproducibility slow down the wide adoption of such a powerful research tool.
This talk introduces how COMET™ performs automated staining and imaging, achieving high-quality, reproducible, and consistent results thanks to the Fast Fluidic Exchange™ (FFeX™) microfluidic technology.
