Yes. These liver-derived macrophages act as a robust in vitro surrogate for Kupffer cells. They sense DAMPs and PAMPs, respond strongly to endotoxin and hepatotoxic compounds, and release key mediators such as TNF-α, IL-1β, and IL-6.
When the recommended rapid-thaw procedure is followed, post-thaw viability typically exceeds 90%, and cells attach and spread within several hours. Deviations such as slow thawing, prolonged exposure to DMSO, or delayed seeding can reduce viability and impair adherence. We supply a detailed thawing and recovery protocol, including suggested centrifugation steps and seeding densities, to help you maintain optimal morphology and function for both short- and multi-day experiments.
The cells attach well to standard tissue-culture-treated plastic, which is sufficient for most ELISA, qPCR, and cytokine-release assays. For high-content imaging, long-term cultures, or frequent washing steps, we recommend collagen, fibronectin, or similar ECM coatings to enhance adherence and spreading.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.