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. Author manuscript; available in PMC: 2015 Jun 29.

Published in final edited form as: Clin Cancer Res. 2007 Jun 1;13(11):3235–3243. doi: 10.1158/1078-0432.CCR-06-2608

Fig. 1 — Experiment varying the amount of A908 WT and mutant A908G ERα plasmid DNAs which were sequenced using SNaPshot™ (panels A, C, E, G, I, K) and dye-labeled terminator (panels B, D, F, H, J, L) with reverse sequencing primers. The TTCT (WT) and TTCC (Mut) base pair combination is overlined, and the WT or mutant C 908 reverse strand bases are underlined.

Fig. 1 — Experiment varying the amount of A908 WT and mutant A908G ERα plasmid DNAs which were sequenced using SNaPshot™ (panels A, C, E, G, I, K) and dye-labeled terminator (panels B, D, F, H, J, L) with reverse sequencing primers. The TTCT (WT) and TTCC (Mut) base pair combination is overlined, and the WT or mutant C 908 reverse strand bases are underlined.