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. Author manuscript; available in PMC: 2017 Dec 27.
Published in final edited form as: Eur Cell Mater. 2017 Dec 5;34:341–364. doi: 10.22203/eCM.v034a21

Fig. 2.

Fig. 2

The lateral femoral condyles of rabbit distal femora were decalcified in EDTA, bisected and the halves embedded in paraffin. Sagittal sections of the condyle halves were stained with safranin O/fast green and haematoxylin. Stitched images of the whole surface, as well as four higher-magnification images, were scored according to the system of Laverty et al. (2010): the stitched images were used to score GAG staining and surface structure, while the higher magnification images were used to determine chondrocyte density and clustering.