Abstract
This chapter describes quantitative methods for isolating and culturing rodent osteoclasts on dentine, a bone-like, resorbable substrate. These techniques generate relatively large numbers of osteoclasts and allow the key processes of osteoclast formation and activation to be studied independently. A special focus will be on the role of extracellular pH, a critical factor in the control of osteoclast function.
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APA
Orriss, I. R., & Arnett, T. R. (2012). Rodent osteoclast cultures. Methods in Molecular Biology, 816, 103–117. https://doi.org/10.1007/978-1-61779-415-5_8
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