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
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
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
Representative images in the revised S2C Fig were generated from raw files woGF_4_ch1/2 (W/O GF); EF10cyc_4_ch1/2 (E+F10+Cyc); EF1shh_7_ch1/2 (E+F1+Shh). (ZIP)
