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. 2011 Jun 8;301(4):C862–C871. doi: 10.1152/ajpcell.00479.2010

Fig. 10.

Fig. 10.

Zip14-dependent Ca2+ uptake and the effects of divalent metal ions. A: uptake of 150 μM 45Ca2+ in the absence (None) or presence of 30 μM Fe2+ or 30 μM Cd2+ in control oocytes (gray bars) and oocytes expressing Zip14 (black bars, n = 9–12) in media containing 1 mM l-ascorbic acid and 100 μM niflumic acid. Two-way ANOVA revealed an interaction (P < 0.001); within Zip14, anot significant (unadjusted P = 0.68) and bP < 0.001 cf. “None”. B: uptake of 300 μM 45Ca2+ in the absence (None) or presence of 15 μM Zn2+ in control oocytes (gray bars) and oocytes expressing Zip14 (black bars, n = 12–13) in media containing 100 μM niflumic acid. Two-way ANOVA revealed an interaction (P < 0.001).