Figure 4
Figure 4. Leukemia cell death assay. Untreated OCI-AML3 cells served as a control to determine the background levels of cell death under the experimental conditions used. Cells were incubated with 20μM CGFYWLRSC + D(KLAKLAK)2 control peptide or with 20μM CGFYWLRSC-GG-D(KLAKLAK)2 for 20 hours at 37°C. annexin V–FITC/propidium iodide staining was used to detect the level of cell death via flow cytometry.

Leukemia cell death assay. Untreated OCI-AML3 cells served as a control to determine the background levels of cell death under the experimental conditions used. Cells were incubated with 20μM CGFYWLRSC + D(KLAKLAK)2 control peptide or with 20μM CGFYWLRSC-GG-D(KLAKLAK)2 for 20 hours at 37°C. annexin V–FITC/propidium iodide staining was used to detect the level of cell death via flow cytometry.

Close Modal
This Feature Is Available To Subscribers Only

or Create an Account

Close Modal
Close Modal