It typically supports baseline differentiation plus a focused set of stimulation conditions (e.g., M0 vs. one polarization arm with technical replicates), or a smaller co-culture proof-of-concept. It's also a good choice if you want to validate your protocol and readouts before scaling to 2.5 × 10^7 or 5 × 10^7 formats.
Yes. Many teams differentiate CD14+ monocytes into macrophages and then assess functional endpoints such as phagocytosis. To improve interpretability, we recommend including a consistent recovery period post-thaw, standardizing differentiation days, and running a baseline phenotype check before the functional assay. This reduces the risk that a transient post-thaw stress state influences uptake behavior or cytokine background.
Keep processing time tight, handle gently, avoid harsh centrifugation, and never refreeze. Because the vial size is optimized for single-run use, designing your workflow so the vial is consumed in one controlled experiment generally yields the best recovery and data consistency. Follow the receiving guidance: immediate LN2 storage upon arrival and minimal temperature fluctuation.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.