Fig. 4.
Fig. 4. Effects of cell culture temperature on viable cell number, morphology, and cell surface phenotype of JKB p16MT cells. (A) JKB p16MT cells were cultured under the following conditions: 40°C for 7 days (□); 31°C for 7 days (▪); 31°C for 1 day, then 40°C for 6 days (○); 31°C for 2 days, then 40°C for 5 days (⊞); 31°C for 3 days, then 40°C for 4 days (×); and 31°C for 4 days, then 40°C for 3 days, ( —  ▴  — ). JKB control cells were cultured at either 40°C (▵) or 31°C (•) for 7 days. Viable cell number was assessed using trypan blue staining. (B) JKB control (left) and JKB p16MT cells (right) were cultured at 40°C (upper) or 31°C (lower) for 7 days. Cell cytosmears were stained with Wright-Giemsa solution. / (C) JKB control (left) and JKB p16MT (right) cells were cultured at 40°C (upper) or 31°C (lower) for 7 days. Cell surface phenotype was determined by flow cytometric analysis.

Effects of cell culture temperature on viable cell number, morphology, and cell surface phenotype of JKB p16MT cells. (A) JKB p16MT cells were cultured under the following conditions: 40°C for 7 days (□); 31°C for 7 days (▪); 31°C for 1 day, then 40°C for 6 days (○); 31°C for 2 days, then 40°C for 5 days (⊞); 31°C for 3 days, then 40°C for 4 days (×); and 31°C for 4 days, then 40°C for 3 days, ( —  ▴  — ). JKB control cells were cultured at either 40°C (▵) or 31°C (•) for 7 days. Viable cell number was assessed using trypan blue staining. (B) JKB control (left) and JKB p16MT cells (right) were cultured at 40°C (upper) or 31°C (lower) for 7 days. Cell cytosmears were stained with Wright-Giemsa solution.

(C) JKB control (left) and JKB p16MT (right) cells were cultured at 40°C (upper) or 31°C (lower) for 7 days. Cell surface phenotype was determined by flow cytometric analysis.

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