Fig. 2.
Fig. 2. EPO expression in CD34+ cells. (A) Bone marrow cells were first enriched for CD34+ cells by magnetic sorting.22 Cells were further separated by fluorescence-activated cell sorting by using phycoerythrin-labeled anti-34 antibody recognizing a different CD34 epitope and cocktail of anti-lin (CD2, CD14, CD15, CD16, CD19, and glycophorin) antibodies labeled with fluorescein isothiocyanate. CD34+lin− (R1) and CD34+lin+ (R2). (B) Total RNA from separated cells (4 × 104 of CD34+lin− and 1 × 104 of CD34+lin+) was prepared for RT-PCR (35 cycles) with EPO and G6PD primers (CD34+lin− cDNA template was prepared from 4 times more cells than CD34+lin+ cDNA, which resulted in higher genomic DNA contamination detected by PCR). CD34+lin+ cells (lane R2) contain EPO mRNA, whereas CD34+lin− do not (lane R1). Size marker 123 bp ladder (M), negative control (−), genomic DNA (g), EPO and G6PD cDNA (+).

EPO expression in CD34+ cells. (A) Bone marrow cells were first enriched for CD34+ cells by magnetic sorting.22 Cells were further separated by fluorescence-activated cell sorting by using phycoerythrin-labeled anti-34 antibody recognizing a different CD34 epitope and cocktail of anti-lin (CD2, CD14, CD15, CD16, CD19, and glycophorin) antibodies labeled with fluorescein isothiocyanate. CD34+lin (R1) and CD34+lin+ (R2). (B) Total RNA from separated cells (4 × 104 of CD34+lin and 1 × 104 of CD34+lin+) was prepared for RT-PCR (35 cycles) with EPO and G6PD primers (CD34+lin cDNA template was prepared from 4 times more cells than CD34+lin+ cDNA, which resulted in higher genomic DNA contamination detected by PCR). CD34+lin+ cells (lane R2) contain EPO mRNA, whereas CD34+lin do not (lane R1). Size marker 123 bp ladder (M), negative control (−), genomic DNA (g), EPO and G6PD cDNA (+).

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