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Experiment Overview

Repository ID: FR-FCM-Z8EP Experiment name: Viable Cell Barcoding with SeMal and TeMal MIFlowCyt score: 51.50%
Primary researcher: Marie Iannone PI/manager: Marie Iannone Uploaded by: Marie Iannone
Experiment dates: 2023-03-01 - 2023-03-31 Dataset uploaded: Oct 2024 Last updated: Oct 2024
Keywords: [mass cytometry] [CyTOF] [SeMal] [TeMal] [selenium maleimide] [tellurium maleimide] [mass-tag cell barcoding] Manuscripts: [39582135] Cytalogo
Organizations: University of North Carolina at Chapel Hill, Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina (USA)
Purpose: Pooled Antibody Staining of Viable PBMC after SeMal/TeMal 21-plex Barcoding. Twenty-one individual PBMC samples (PBMC from seven separate donors with 3 replicates per donor) were barcoded using the SeMal/TeMal isotope scheme shown in Figure 5A and Supplemental Figure S5A of publication 24-120.R1 Cytometry Part A. The barcoded samples were mixed, viability stained then incubated, as a pool, with a pre-titrated 33-marker antibody cocktail (See Supplemental Table S1 for list of markers and metals). After surface marker staining, cells were fixed with 1.6% paraformaldehyde and incubated with iridium overnight.
Conclusion: Each donor sample replicate retained its unique phenotypic profile with excellent reproducibility.
Comments: Data used in Figure 6 of publication 24-120.R1 Cytometry Part A.
Funding: Not disclosed
Quality control: This is a bead normalized fcs file.
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