Yes, with smart prioritization. Use miniaturized formats (96/384 well), reduce "nice-to-have" conditions, and reserve a small fraction for a quick standard curve. We can help you map a design that hits your key hypotheses while staying within cell constraints.
Build a simple standardization framework: consistent cell number per well, fixed substrate concentration and incubation time, and a calibration curve (serial dilution of cells) on every plate. If you're differentiating into macrophages first, calibrate at the same differentiation day you'll use for the real experiment.
Yes. Many teams first use luciferase to quantify kinetics, then switch to phenotype/function assays (cytokines, phagocytosis, antigen presentation, polarization markers) for mechanism. If you want an integrated plan, we can propose a staged workflow so tracking and function tell a consistent story.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.