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. 2000 Jul;20(14):5227–5234. doi: 10.1128/mcb.20.14.5227-5234.2000

FIG. 4.

FIG. 4

Phosphorylation of NFATc1-α in vivo. (A) NFATc1-α was coexpressed with MKK7 plus JNK1 in COS cells. The effect of replacement of Ser117 and Ser172 with Ala residues was investigated. Cell lysates were examined by protein immunoblot analysis by sequentially probing with anti-phospho-NFATc1-α and anti-NFATc1. A nonspecific band was detected by the phospho-NFATc1-α antibody immediately above the NFATc1-α band. (B) NFATc1-α was coexpressed without (−) and with (+) the JNK inhibitor JIP-1 in COS cells. The cells were treated without (−) and with (+) UV-C radiation (80 J/m2) and harvested after 30 min. The effect of replacement of the JNK phosphorylation sites (Ser117 and Ser172) with Ala was examined. The NFATc1-α proteins were detected by protein immunoblot analysis by sequentially probing with anti-phospho-NFATc1-α and anti-NFATc1.