A novel and rapid apoptosis assay based on thiol redox status
Article first published online: 7 MAR 2012
Copyright © 2012 International Society for Advancement of Cytometry
Cytometry Part A
Volume 81A, Issue 5, pages 430–436, May 2012
How to Cite
Skindersoe, M. E., Rohde, M. and Kjaerulff, S. (2012), A novel and rapid apoptosis assay based on thiol redox status. Cytometry, 81A: 430–436. doi: 10.1002/cyto.a.22032
- Issue published online: 19 APR 2012
- Article first published online: 7 MAR 2012
- Manuscript Accepted: 13 FEB 2012
- Manuscript Revised: 6 FEB 2012
- Manuscript Received: 17 NOV 2011
Additional Supporting Information may be found in the online version of this article.
|CYTO_22032_sm_SuppFigS1.doc||45K||Supporting Information Figure S1. Staining kinetics and fluorescence intensities of VitaBright-48 and monochlorobimane. The histograms show the fluorescence intensity of Jurkat cells stained with 50 μM VitaBright-48 (left) or 50 μM monochlorobimane (right) and incubated at room temperature as follows: Black line; 1 minute, red line; 2 minutes, blue line 5 minutes, pink line; 10 minutes and green line 15 minutes. Nonviable cells have been gated out based propidium iodide uptake.|
|CYTO_22032_sm_SuppFigS2.doc||2723K||Supporting Information Figure S2. Corresponds to figure 2 with all channels expanded to single channels. Jurkat and WEHI-S cells treated with 25 μM CPT (Jurkat cells) or 100 ng/mL TNF α (WEHI-S cells) and controls. Cells are stained with VitaBright-48, annexin V-CF647 and SYTOX green or VitaBright-48 and FLICA reagent as mentioned in the figure. Last panel shows super-imposition of all channels. Scale bar 25 μm.|
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