Description

SECTION 2: KEY FEATURES (10 Bullets)

• Run Multiple Shaker Experiments Simultaneously with 500 pound total capacity supporting up to 4 orbital shakers on reinforced shelving, enabling parallel CHO cell culture optimization and antibody production screening in a single controlled environment
• Eliminate Temperature Fluctuations During Shaking through enhanced refrigeration that automatically compensates for heat generated by continuous orbital agitation, maintaining ±0.3°C uniformity even with multiple shakers running at 200 RPM
• Power Your Shakers Safely Inside the Chamber with three GFCI-protected electrical outlets eliminating cable routing through door seals that compromise CO2 control and contamination prevention
• Install Without Rigging or Facility Modifications as the 7401-25 rolls through standard 36-inch doorways despite heavy-duty construction, reducing installation costs and downtime compared to larger bioprocessing equipment
• Scale From Shake Flasks to Production Bioreactors within the 20-60°C temperature range supporting bacterial fermentation at 37°C, mammalian cell culture at 37°C, and yeast cultivation at elevated temperatures in the same versatile platform
• Reconfigure Platforms Between Campaigns in Minutes using tool-free interior disassembly to switch from shake flask arrays to roller bottle configurations to wave bioreactor setups without requiring technical service calls
• Sterilize Without Removing Your Shaker Platforms through patented 2-hour dry H2O2 cycle achieving 12-log reduction with shakers in place, eliminating time-consuming equipment removal and reinstallation between production runs
• Maximize Throughput With 4x Benchtop Capacity accommodating 40+ shake flasks or 100+ roller bottles in 25 cubic feet, replacing multiple benchtop incubators with a single production-scale unit for streamlined operations and reduced footprint
• Monitor Critical Process Parameters in Real-Time using multiple access ports for dissolved oxygen probes, pH sensors, and sampling lines while maintaining chamber integrity for advanced bioprocess control and optimization
• Meet FDA and cGMP Requirements Out of the Box with validatable sterilization, optional 316 stainless steel cleanroom construction, IQ/OQ documentation support, and 21 CFR Part 11 compatible data logging for compliant biopharmaceutical manufacturing