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. Author manuscript; available in PMC: 2013 Sep 11.
Published in final edited form as: Spine (Phila Pa 1976). 2010 Jun 1;35(13):1257–1264. doi: 10.1097/BRS.0b013e3181c2a8b0

Figure 2.

Figure 2

The chordoma cells were cultured in different commercial available tissue culture media and collagen substrate, and their proliferate activity was evaluated by MTT and numerication assay. A, MTT assay indicated that the CH 8 cells proliferated less actively in RPMI medium and more actively in DMEM and IMDM media. B, MTT assay indicated that the GB 60 cells proliferated less actively in RPMI medium and more actively in DMEM and IMDM media. C, MTT assay indicated that the U-CH1 cells proliferated less actively in RPMI medium and more actively in DMEM medium. D, Cell numeration assay indicated that all 3 chordoma cell lines universally grew better in collagen substrate than collagen free plate.