Fig. 5.
Fig. 5. RT-PCR and Northern blot analyses of TM and TF mRNA in U937 cells and monocytes treated with 1,25(OH)2D3. Total RNA was extracted from cultured U937 cells and monocytes after exposure to 0.1 μmol/L of 1,25(OH)2D3 (lane 2) for 5 hours. RT-PCR analysis of TM (A) or TF (B) mRNA and Northern blot analysis of TM mRNA (C) were performed as described in Materials and Methods. Base-pair markers are shown to the left. GAPDH and β-actin were used as quality controls of mRNA.

RT-PCR and Northern blot analyses of TM and TF mRNA in U937 cells and monocytes treated with 1,25(OH)2D3. Total RNA was extracted from cultured U937 cells and monocytes after exposure to 0.1 μmol/L of 1,25(OH)2D3 (lane 2) for 5 hours. RT-PCR analysis of TM (A) or TF (B) mRNA and Northern blot analysis of TM mRNA (C) were performed as described in Materials and Methods. Base-pair markers are shown to the left. GAPDH and β-actin were used as quality controls of mRNA.

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