• Viabilities routinely >80%
  • Characterized for phase I and phase II enzyme activities

Our mouse hepatocytes are prepared using the same careful isolation and cryopreservation techniques as our human lots.  Characterization methods of cryopreserved hepatocytes include ECOD, 7-HCG and 7-HCS for phase I and phase II enzyme activities.  We also closely monitor cell morphology, attachment efficiency, monolayer confluency (plateable cells) and viability stability over time for cryopreserved hepatocytes.