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. 1998 Mar 17;95(6):2914–2919. doi: 10.1073/pnas.95.6.2914

Figure 7.

Figure 7

[14C]β-d-Glc-IPM uptake into suspended human carcinoma T84 cells, which is mediated by a phlorizin-sensitive transporter. (a) The time course of the phlorizin-inhibitable uptake of 0.2 mM [14C]β-d-Glc-IPM measured in the presence of sodium. (b) The substrate dependence of the initial phlorizin-inhibitable uptake rate of [14C]β-d-Glc-IPM, which was measured in the presence of Na+. Mean values ± SEM from four separate determinations are shown. In the presence of 0.5 mM phlorizin, nonspecific uptake of [14C]β-d-Glc-IPM was measured, which increased linearly with time and substrate concentration. The nonspecific uptake rate of [14C]β-d-Glc-IPM was 73 ± 2 pmol × mg −1 mM−1 min−1.