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Description

Microsome fraction was prepared by sequential centrifugation (1000 g, 12,000 g, and 120,000 g) of the isotonized cell homogenates

Alternatively, 3050 age-synchronized worms were collected in microfuge tubes and rinsed once with M9 buffer

7 murine macrophages through the MyD88-dependent signaling pathway

Ethics declarations Conflict of interest No authors of this manuscript received funding or grants in support of the research or preparation of the manuscript