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. 2011 Feb 24;135(3):263–280. doi: 10.1007/s00418-011-0793-3

Fig. 4.

Fig. 4

Micrographic pictures showing the intranuclear localization of phospho-Chk1S317 in HeLa cells; control (aa′), a negative control section incubated with secondary antibodies only (bb′), cells incubated for 24 h with 2.5 mM hydroxyurea (cc′), cells incubated for 24 h with 10 mM hydroxyurea (dd′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with 5 mM caffeine (ee′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with the mixture of 2.5 mM hydroxyurea and 5 mM caffeine (ff′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with 10 mM 2-aminopurine (gg′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with the mixture of 2.5 mM hydroxyurea and 10 mM 2-aminopurine (hh′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with 200 nM staurosporine (ii′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with the mixture of 2.5 mM hydroxyurea and 200 nM staurosporine (jj′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with 200 μM sodium metavanadate (kk′), cells incubated for 24 h with 2.5 mM hydroxyurea and post-treated with the mixture of 2.5 mM hydroxyurea and 200 μM sodium metavanadate (ll′). Scale bar = 10 μm