Figure 5
Myr induces apoptosis and reduction of proliferation in lymphoma cells in vitro experiments. (A,D) Daudi and Raji lymphoma cells were treated with etoposide (40μM) for 12 hours and/or Myr (50μM) for 24 hours as indicated and then analyzed by MTS assay. Bar graphs show SD for values from 3 experiments (*P < .05, **P < .005). (C,F) Daudi and Raji lymphoma cells were treated with etoposide (40μM) for 12 hours and/or Myr (50μM) for 24 hours as indicated and then analyzed by TUNEL analysis. Bar graphs show SD for values from 3 experiments (*P < .05, **P < .005). (B,E) Cells lysates from described experiment were immunoblotted with anti-Tcl1, anti-Parp, and anti-Gapdh antibodies.

Myr induces apoptosis and reduction of proliferation in lymphoma cells in vitro experiments. (A,D) Daudi and Raji lymphoma cells were treated with etoposide (40μM) for 12 hours and/or Myr (50μM) for 24 hours as indicated and then analyzed by MTS assay. Bar graphs show SD for values from 3 experiments (*P < .05, **P < .005). (C,F) Daudi and Raji lymphoma cells were treated with etoposide (40μM) for 12 hours and/or Myr (50μM) for 24 hours as indicated and then analyzed by TUNEL analysis. Bar graphs show SD for values from 3 experiments (*P < .05, **P < .005). (B,E) Cells lysates from described experiment were immunoblotted with anti-Tcl1, anti-Parp, and anti-Gapdh antibodies.

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