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Resolution: standard / high Figure 4.
Subcellular localization of RNF122. (A) HeLa or HEK293T cells were grown on coverslips and transfected with RNF122-N1
and CAML-FLAG. To inhibit the degradation of RNF122-N1, the cells were treated with
2.5 μM MG132 for 6 h. The cells were then treated with anti-FLAG antibody and FITC-conjugated
goat anti-mouse antibody, and observed under a confocal microscopy. The results showed
that the cytoplasmic distribution of CAML entirely overlapped that of RNF122. (B)
HEK293T cells were transfected with RNF122-N1 and RNF122ΔTM-N1 and observed under
a fluorescence microscope.
Peng et al. BMC Cell Biology 2010 11:41 doi:10.1186/1471-2121-11-41 |