Figure 4
Figure 4. Expression profiles of SAMHD1 in primary CLL cells. (A) cDNA pools from B cells (CD19+, CD5−) sorted from peripheral blood of healthy donors and SAMHD1-mutated CLL cells (CD19+, CD5+) were subjected to quantitative PCR analysis using ABL as a control gene. (B) Measurement of SAMHD1 mRNA by quantitative RT-PCR. The percentage of leukemia cells (CD5+/CD19+) is indicated. Statistical comparison of SAMHD1 mRNA levels between each CLL sample and the mean of the healthy PBMCs was performed. The black bars indicate P < .01. (C) Measurement of SAMHD1 protein levels by western blot in 10 CLL samples and 7 healthy PBMCs. Ponceau dye staining was used to control protein load.

Expression profiles of SAMHD1 in primary CLL cells. (A) cDNA pools from B cells (CD19+, CD5) sorted from peripheral blood of healthy donors and SAMHD1-mutated CLL cells (CD19+, CD5+) were subjected to quantitative PCR analysis using ABL as a control gene. (B) Measurement of SAMHD1 mRNA by quantitative RT-PCR. The percentage of leukemia cells (CD5+/CD19+) is indicated. Statistical comparison of SAMHD1 mRNA levels between each CLL sample and the mean of the healthy PBMCs was performed. The black bars indicate P < .01. (C) Measurement of SAMHD1 protein levels by western blot in 10 CLL samples and 7 healthy PBMCs. Ponceau dye staining was used to control protein load.

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