The storage requirements are the same as smaller formats: immediate transfer to liquid nitrogen upon receipt and avoidance of repeated freeze-thaw. For larger vials, planning is even more important-prepare media, plates, and counting reagents in advance so the cells spend minimal time in transitional temperatures. If you need partial usage, we recommend designing the experiment to consume the entire vial in one controlled run rather than attempting refreezing.
Yes. 5 × 10^7 cells per vial is specifically advantageous when your design requires multiple timepoints, replicate conditions, or high-input workflows (e.g., RNA extraction after stimulation, parallel secretome profiling, or multi-panel flow). The larger format helps you keep conditions within the same donor lot to reduce biological variance.
Absolutely. Many clients use a standard monocyte-to-macrophage workflow but adjust seeding based on plate format, stimulation duration, and endpoint sensitivity. If you tell us your plate type (6/12/24/96-well), the macrophage phenotype target, and readouts (ELISA, flow, imaging, RNA-seq), we can suggest a practical seeding and timeline plan to optimize yield and signal-to-noise-without over-consuming cells.
For Research Use Only. Do Not Use in Food Manufacturing or Medical Procedures (Diagnostics or Therapeutics). Do Not Use in Humans.