In many workflows, reporter signal remains detectable through differentiation, but intensity can shift with activation state, culture duration, and instrument settings. We recommend a short pilot: thaw, recovery, differentiation, stimulus panel, then lock exposure/gating parameters. If you need higher-confidence tracking, we can suggest complementary approaches (e.g., dual readouts with surface markers).
Handle as a cryopreserved product: ship on dry ice, transfer to liquid nitrogen immediately on arrival, and avoid repeated freeze-thaw cycles. These steps help preserve both viability and functional performance.
Yes. Many teams run GFP+ and wild-type monocytes in parallel to confirm the label doesn't influence the phenotype of interest. Share your study goal, and we'll recommend a matched control strategy that keeps interpretation tight and publication-ready.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.