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. 2005 May 3;102(19):6984–6989. doi: 10.1073/pnas.0502097102

Fig. 3.

Fig. 3.

Analysis of BMP9-induced proteins. (Upper) Western blots of selected proteins from control and BMP9-treated neuronal cultures. Septal cultures from E14 mice were treated for 3 days with BMP9 (10 ng/ml) or vehicle. Cells were harvested and processed for SDS/PAGE as described in Materials and Methods. (Lower) Immunocytochemistry (AJ) of cultures are treated as in Upper.(AD) Double immunofluorescence staining with anti-Na+/K+ ATPase α-1 and anti-VACHT antibodies, done in parallel with negative and positive controls. (E and F) Immunofluorescence staining with anti-NGFR antibody. Phase-contrast (G and H) and immunofluorescence (I and J) staining with anti-Noggin antibody of the same field. All pictures were obtained with a ×20 objective.