We recommend a rapid, controlled thaw followed by stepwise dilution into pre-warmed medium to reduce osmotic shock. To keep baselines consistent across plates, lock seeding density, medium composition, and the timing of cytokine additions or stimuli.
Yes. We can support monocyte-to-macrophage differentiation under defined cytokine conditions, optional polarization into defined activation states, and fit-for-purpose validation readouts. Typical deliverables can include phenotyping guidance or verification, cytokine profiling, and functional checks such as phagocytosis or stimulus-response assays, depending on your study.
Most performance issues are driven by controllable variables rather than the cells themselves-thaw speed, wash intensity, density, recovery time, medium, or stimulation schedule. We troubleshoot quickly by reviewing your protocol and endpoints, then proposing targeted changes. Our goal is to get you back to decision-quality data with minimal repeats.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.