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Data · dataset · 2022

Chromium Next GEM Single Cell 3’ RNA-sequencing of tumor cell line co-cultured with PBMC and treated with trifluridine or DMSO control

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Chromium Next GEM Single Cell 3’ RNA-sequencing.

Description

HCT116 were seeded in 6-well Nunc plates (50,000 cells/3mL/well) and precultured for 24 h before PBMCs were added at a 1:8 ratio. Co-cultures were treated with DMSO vehicle (0.1%) or FTD (3mM) for 12 h or 72 h.

MACS Dead Cell Removal Kit (Miltenyi Biotec, Gladbach, DEU) was performed according to the manufacturer’s instructions on cells treated for 72 h to increase the viability of the samples before RNA-sequencing. The viability of the samples treated for 12 h was not subjected to Dead Cell Removal as the viability was already sufficient. All samples were washed in PBS with 0.04% BSA (2x1mL).

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Chromium Next GEM Single Cell 3’ library preparation and RNA-sequencing were performed by the SNP&SEQ Technology Platform (National Genomics Infrastructure (NGI), Science for Life Laboratory, Uppsala University, Sweden).

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Where it is published

Catalogue records · 1

Topics

Inferred from text
Cancer 65% · Oncology and carcinogenesis 69%
Provenance · 1 source records, 9 field assertions
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Researchdata.seoai:researchdata.se:doi-10-17044-scilifelab-19761343/013 d agoJSON v1
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concepts[field].anzsrc:group:3211enrichment · researchdata setaxonomy-embedding@1.1.0title+keywords+description (69%)
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concepts[field].local:field:medicine-healthmapping · researchdata seconnector:researchdata_se@1.0.0
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