Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy

Publication date

2021-09-17

Authors

Segeren, Hendrika AISNI 0000000492798653
Andree, Kiki C
Oomens, Lisa
Westendorp, BartORCID 0000-0003-1043-3638ISNI 0000000396403121

Editors

Advisors

Supervisors

Document Type

Article
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License

cc_by

Abstract

FACS sorting followed by single-cell RNA-sequencing (SORT-Seq) is a popular procedure to select cells of interest for single-cell transcriptomics. However, FACS is not suitable for measurement of subcellular distribution of fluorescence or for small samples (<1,000 cells). The VYCAP puncher system overcomes these limitations. Here, we describe a workflow to capture, image, and collect fluorescent human retina pigment epithelium cells for SORT-Seq using this system. The workflow can be used for any cell type with a diameter of ∼5-50 μm. For complete details on the use and execution of this protocol, please refer to Segeren et al. (2020).

Keywords

Cell Biology, Genomics, Microscopy, Single Cell, General Biochemistry,Genetics and Molecular Biology, General Neuroscience, General Immunology and Microbiology

Citation

Segeren, H A, Andree, K C, Oomens, L & Westendorp, B 2021, 'Collection of cells for single-cell RNA sequencing using high-resolution fluorescence microscopy', STAR Protocols, vol. 2, no. 3, 100718, pp. 1-11. https://doi.org/10.1016/j.xpro.2021.100718