Figure 1.
Figure 1. Effects of CD44 ligation on the proliferation and cell cycle status of NB4 cells. (A) NB4 cells (105/mL) were seeded in 96-well culture plates in complete culture medium containing anti-CD44 mAb A3D8 (2.5 μg/mL) and were cultured for 5 days at 37°C. Control cells were cultured with IgG1. Cell numbers and viability were evaluated by the trypan blue exclusion test. Data are means ± 1 SD calculated from 3 independent experiments using triplicate samples. This figure is from Charrad et al.19 (B) Cells were treated with IgG1 or A3D8 for 48 hours, and cell cycling was analyzed by flow cytometry (Multicycle program) after propidium iodide (PI) staining. G0/G1 represents Gap 0/Gap1 phase; S, DNA synthesis phase; and G 2/M, mitosis phase. Results represent 1 representative experiment of 3. Values are means ± 1 SD resulting from quadruplicate samples.

Effects of CD44 ligation on the proliferation and cell cycle status of NB4 cells. (A) NB4 cells (105/mL) were seeded in 96-well culture plates in complete culture medium containing anti-CD44 mAb A3D8 (2.5 μg/mL) and were cultured for 5 days at 37°C. Control cells were cultured with IgG1. Cell numbers and viability were evaluated by the trypan blue exclusion test. Data are means ± 1 SD calculated from 3 independent experiments using triplicate samples. This figure is from Charrad et al.19  (B) Cells were treated with IgG1 or A3D8 for 48 hours, and cell cycling was analyzed by flow cytometry (Multicycle program) after propidium iodide (PI) staining. G0/G1 represents Gap 0/Gap1 phase; S, DNA synthesis phase; and G 2/M, mitosis phase. Results represent 1 representative experiment of 3. Values are means ± 1 SD resulting from quadruplicate samples.

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