It supports both. Imaging is the obvious benefit, but GFP is also valuable for cell recovery and gating during differentiation (e.g., distinguishing your macrophage lineage from other populations in mixed systems). To keep signals clean, we recommend aligning filter sets/compensation early and defining a consistent gating template before scaling experiments.
Use gentle handling: rapid thaw, gradual dilution, minimal centrifugation force, and immediate placement into optimized culture conditions. The page explicitly warns against repeated freeze-thaw and instructs liquid-nitrogen storage upon receipt-those steps matter directly for recovery.
Fluorescent intensity can vary with activation state, culture stress, and imaging settings. To protect interpretability, design your analysis around relative changes (within-run controls) and consider reporting both percent GFP+ and median fluorescence intensity (MFI) where relevant. If you share your planned endpoints, we can suggest an acquisition/analysis strategy that fits your platform.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.