Yes. CD14+ monocytes are a common precursor for macrophage differentiation, and having a cryopreserved, flow-characterized starting population helps standardize your baseline before polarization (e.g., classically activated vs alternative activation-like conditions). With 5×10^7 cells/vial, you can run differentiation plus phenotype/functional panels without constant resourcing interruptions.
For time-course designs, consistency is everything: thaw once, seed all time points in parallel when feasible, and keep media and stimulation timing tightly controlled. If your study spans weeks, securing sufficient vials from the same lot reduces variability. We can also advise on an allocation plan that preserves enough cells for QC at each stage.
Upon receipt, transfer the vial directly from dry ice to liquid nitrogen storage (-150°C to -190°C). Temperature excursions can compromise viability; the handling notes emphasize that viability cannot be guaranteed if the recommended procedure is not followed.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.