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After achieving 80–90% confluence, the cells were cultured in a variety of methods by a variety of experimental protocols: 1 × 10 6 cells were plated on a 6-well plate to study the inflammatory marker and the intracellular pathways by ELISA kit
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Dosage:1mg (standard)
Deleting RBF1 ( CPAR2_600470 ) resulted in poor growth on arginine, GABA, glutamate, glutamine, and glycine (Supplementary Fig
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