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. Author manuscript; available in PMC: 2015 Jul 17.
Published in final edited form as: Immunity. 2014 Jul 17;41(1):14–20. doi: 10.1016/j.immuni.2014.06.008

Table 1.

Reporting standards for in vitro experiments

Parameter Notes
Mouse strain How was the bone marrow isolated and processed?
Starting cell number, media and supplements Media (DMEM versus RPMI) has substantial effects of growth rate, development and activation status
Tissue culture conditions Different types of plastic affect macrophage growth and activation. Tissue culture conditions should be documented for reproducibility
Time of culture What were the precise conditions used? Were cytokines and/or media supplemented during the culture period
Source and concentration of differentiation cytokines The source and concentration of CSF-1
Macrophage yield The yield relative to the starting number should be recorded
Activation conditions Variables include whether the macrophages were rested prior to activation and how, whether CSF-1 was present in the activation cultures, the source and concentrations of the activating agents, and the time to assay
Processing and analysis How were the cells processed, and what marker readouts used