The in situ detection of caspase-3 activity has applications in the imaging and monitoring of multiple pathologies, notably cancer. A series of cell penetrating FRET-based fluorogenic substrates were
Plasma-treated and H2O2 exposed cells were cultured for 1, 6, 12, 24, and 48 hrs. Cells were then stained with Annexin-V (A) and propidium iodide (PI) and evaluated by FACS analysis to assess cell dea
Cells (2×10 5 ) were cultured in 6-well plates, and then were incubated with sunitinib for 24 hr. Necrosis was analyzed using the Annexin V-FITC/PI Apoptosis Detection Kit (40302ES50, Yeasen
Raw caspase activity measurements and code used in Figure S4 of primary Mus fibroblasts of genotypes tested in paper in untreated, irradiated, and neocarzinostatin treated populations. We used the Apo
