RocketCell™ Cell Viability Enhancer (1000X)
Maximize cell recovery and growth during passaging, thawing, and cryopreservation.
Superior Growth Kinetics
Outperforms Y-27632 and Thiazovivin (TZV), in long-term expansion assays.
Metabolic Support
Actively assists cells in recovering from the metabolic stress of detachment and enzymatic dissociation.
Versatile
Optimized for use during passaging, thawing, and cryopreservation to ensure maximum plate-down efficiency.
Proprietary Protection
Contains a potent ROCK inhibitor integrated with secondary metabolic stabilizers to prevent apoptosis and promote rapid cell-cycle re-entry.
RocketCell™ Cell Viability Enhancer is a proprietary, high-potency small-molecule cocktail engineered to maximize the survival and metabolic recovery of sensitive cell types, including, but not limited to, organoids, induced pluripotent stem cells (iPSCs), and other iPSC-derived cells, such as neural stem cells.
While traditional ROCK inhibitors like Y-27632 provide basic survival signals, RocketCell™ Cell Viability Enhancer utilizes a synergistic approach that significantly accelerates post-passaging growth and colony formation. This reagent is designed for 2D and 3D cultures.
Specifications
| Use | Use maximize the survival and metabolic recovery of sensitive cell types. |
| Shipping and Storage | Ships with ice pack or dry ice. Store at -20°C. |
Data and References
Figure 1. RocketCell™ Cell Viability Enhancer Supports Higher Intestinal Organoid Recovery & Growth. Mouse intestinal organoids (MIO) cultured in VitroGel® ORGANOID 5 (at P6) were harvested and passaged using VitroGel® ORGANOID Recovery Solution and TrypLE. Organoid fragments were re-cultured in VitroGel® ORGANOID 5 with or without RocketCell™ Cell Viability Enhancer in RocketCell™ Organoid Xeno-Free Essential-Core Medium with essential growth factors. (A-B) MIO growth without the Cell Viability Enhancer Day 0 vs Day 8, respectively. (C) MIO growth without the RocketCell™ Cell Viability Enhancer video. (D-E) MIO growth with the RocketCell™ Cell Viability Enhancer Day 0 vs Day 8, respectively. (F) MIO growth with the RocketCell™ Cell Viability Enhancer video. (G) MIO growth over 8 days. Use of RocketCell™ Cell Viability Enhancer supported better MIO recovery and growth over 8 days compared to media without RocketCell™ Cell Viability Enhancer.
Figure 2. RocketCell™ Cell Viability Enhancer Supports Higher Colon Organoid Recovery & Growth.
Colon organoids (CO) cultured in Matrigel domes (at P2) were harvested and passaged using TrypLE. Organoid fragments were re-cultured in Matrigel domes with or without Cell Viability Enhancer. (A-B) CO growth without the Cell Viability Enhancer, Day 0 vs Day 8, respectively. (C) CO growth without the Cell Viability
Enhancer video. (D-E) CO growth with the Cell Viability Enhancer Day 0 vs Day 8, respectively. (F) CO growth with the Cell Viability Enhancer video. (G) CO growth over 8 days. Use of RocketCell™ Cell Viability Enhancer supported better CO recovery and growth over 8 days compared to media without RocketCell™ Cell Viability Enhancer.
Figure 3. Effects of RocketCell™ Cell Viability Enhancer (CVE) During Organoid Harvesting: Enhanced Intestinal Organoid Recovery and Growth.
Mouse intestinal organoids (MIOs; passage 3) cultured in Matrigel domes were harvested and passaged using TrypLE. In condition (A), RocketCell™ Cell Viability Enhancer (RCVE) was not included during harvesting, whereas in condition (B), RCVE was used throughout all harvesting steps. Following harvest, organoid fragments were reseeded in Matrigel domes and cultured in RocketCell™ Organoid Xeno-Free Essential-Core Medium supplemented with essential growth factors, either with or without RCVE.
The use of RocketCell™ Cell Viability Enhancer significantly improved MIO recovery and growth over the 4-day culture period compared with cultures maintained without RCVE. The greatest enhancement in organoid recovery and expansion was observed when RCVE was included during harvesting and maintained during the initial 24–48 hours of culture. Furthermore, comparison of panels A3 and B3 demonstrates improved organoid survival when RCVE was used during the harvesting process, even in the absence of RCVE supplementation during the subsequent 24–48 hours of culture. These findings indicate that RCVE provides substantial protection against harvesting-induced cellular stress, leading to improved organoid viability and recovery.

