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. 1998 Mar 3;95(5):2325–2330. doi: 10.1073/pnas.95.5.2325

Figure 5.

Figure 5

Time course of PRL mRNA accumulation in PR1 cells cultured under different conditions. On the indicated day the cells were harvested and total RNA was prepared for PRL Northern blot analysis as described. One nanomole of E2 or ICI was used for treatment. CHOB, a cDNA of ribosomal protein S2, was used as a loading control.