Fig. 2.
Fig. 2. Identification of 1,25(OH)2D3 -modulated genes transcription by DD-RT-PCR. DD-RT-PCR was performed on total RNA from unstimulated (lane C) and 1,25-(OH)2D3 –stimulated neonatal monocytes (lane D) as described in the Materials and Methods using primers T11CA and Ltk3 . Arrows indicate interesting labeled DNA products. Amplified double-stranded DNA corresponding to the amplification of 15-PGDH is noted as “b.” Total RNA samples pretreated by RNase A were used in the same experimental conditions to confirm the absence of genomic DNA contamination (lanes A, untreated cells; lane B, 1,25-(OH)2D3 –treated cells).

Identification of 1,25(OH)2D3 -modulated genes transcription by DD-RT-PCR. DD-RT-PCR was performed on total RNA from unstimulated (lane C) and 1,25-(OH)2D3 –stimulated neonatal monocytes (lane D) as described in the Materials and Methods using primers T11CA and Ltk3 . Arrows indicate interesting labeled DNA products. Amplified double-stranded DNA corresponding to the amplification of 15-PGDH is noted as “b.” Total RNA samples pretreated by RNase A were used in the same experimental conditions to confirm the absence of genomic DNA contamination (lanes A, untreated cells; lane B, 1,25-(OH)2D3 –treated cells).

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