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. Author manuscript; available in PMC: 2014 May 1.
Published in final edited form as: Nat Neurosci. 2013 Sep 22;16(11):1608–1617. doi: 10.1038/nn.3526

Figure 3.

Figure 3

NtBuHA prevents H2O2-induced apoptosis in INCL lymphoblasts. (Panel a) Flow cytometric analysis of apoptotic cells using apoptosis-marker, annexin V and necrotic cells using necrotic cell marker PI: Untreated control INCL lymphoblasts (Upper left panel); NtBuHA-pretreated (Upper middle panel); and NtBuHA pre- as well as co-treated (Upper right panel). INCL lymphoblasts were either untreated and exposed to oxidative-stress by H2O2 (untreated control, Lower left panel) or the cells were first pretreated with NtBuHA for 12h and then incubated with H2O2 in the absence (Lower middle panel) or presence of NtBuHA (Lower right panel) for 3h. (Panel b) Graphical presentation of level of apoptotic cells in untreated and NtBuHA-treated INCL cells. Apoptotic cells represent annexinV positive cells detected by FACS (Summation of cell number in Q2 + Q3).