Yes, with the right differentiation conditions and feeding strategy. For longer cultures, consistency in cytokine supplementation, media refresh cadence, and seeding density becomes critical. We also recommend monitoring morphology and marker expression at defined checkpoints to ensure the phenotype remains aligned to your study goal rather than drifting due to over-confluence or nutrient stress.
Post-thaw viability can vary by donor and handling, but the biggest controllable factors are thaw speed, DMSO exposure time, centrifugation conditions, and whether the cells experience temperature fluctuations. We provide handling guidance to help you protect viability and functional responsiveness. If your assay is especially sensitive, we can advise on a short recovery/rest step before differentiation.
Depending on availability and your study design, we can discuss options to align monocyte-derived macrophages with complementary immune components to build more physiologically relevant systems. If your goal is immune cross-talk modeling, we can help you structure a sourcing and experimental plan that maintains donor consistency where it matters most.
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