Fig. 2a | FUS localization in motor neurons

This item is part of the <b>Figshare Project</b>:<br><b>Early mitochondrial dysfunction revealed across FUS- and TARDBP-ALS at single cell resolution</b><br>From <i>Data Availability Statement</i> for the forthcoming paper in <i>Nature Communications</i> entitled:<b>Single-cell RNA sequencing reveals early mitochondrial dysfunction unique to motor neurons shared across FUS- and TARDBP-ALS</b>"We have deposited all raw and processed RNA sequencing data generated in this study on the NCBI Gene Expression Omnibus (GEO) under the accession number GSE226482. The <i>C9orf72</i>-ALS bulk RNA sequencing data was retrieved directly from the authors of the study.[Items under this Figshare Project contain:] "Scans of fluorescent western blots, raw imaging files from confocal microscopy, the analysis files from Opera Phenix, qPCR data sets, and Seahorse assay result files."--------------------------------------------[Item specific description:]Immunofluorescence for FUS localization. These are confocal images of immunofluorescent stainings of FUS in iPSC-derived motor neurons.The file format is .czi, through the ZEN software (Zeiss). If you wish to view and process .czi files, Zeiss recommends using ImageJ and the ImageJ-based Fiji software package.Information about the file format CZI can be found here: https://www.zeiss.com/microscopy/en/products/software/zeiss-zen/czi-image-file-format.html