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DRETOP ZCQ-50 Gas-Jacketed CO₂ Incubator

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Brand DRETOP
Origin Shanghai, China
Manufacturer Type Direct Manufacturer
Instrument Type Gas-Jacketed CO₂ Incubator
CO₂ Detection Infrared (IR) Sensor
Temperature Control Range & Accuracy RT + 5°C to 60°C
CO₂ Concentration Control Range & Accuracy 0–20% vol, ±0.1% vol
Humidity Control 95% RH ±3% RH
Chamber Capacity 50 L
External Dimensions (W×D×H) 475 × 496 × 735 mm
Internal Dimensions (W×D×H) 345 × 355 × 410 mm
Standard Configuration UV Germicidal Lamp (Optional 90°C High-Temperature Humid Heat Sterilization)

Overview

The DRETOP ZCQ-50 is a precision-engineered gas-jacketed CO₂ incubator designed for reliable, contamination-controlled cell and tissue culture under physiologically relevant conditions. It maintains tightly regulated environmental parameters—temperature (RT + 5°C to 60°C), CO₂ concentration (0–20% vol), and relative humidity (95% RH ±3% RH)—to replicate in vivo microenvironments essential for mammalian cell proliferation, hybridoma antibody production, stem cell expansion, IVF procedures, and toxicology assays. Unlike water-jacketed models, the ZCQ-50 employs direct air heating via embedded heaters within the chamber wall, enabling rapid thermal recovery (<6 min to 37°C after 30-sec door opening) and superior responsiveness during high-frequency access—critical for shared-core facilities and time-sensitive workflows. Its IR-based CO₂ sensing system operates independently of ambient temperature and humidity fluctuations, eliminating oxygen dependency and catalytic sensor poisoning common in thermal conductivity (TC) or electrochemical sensors.

Key Features

  • Gas-jacketed heating architecture with nickel-chromium alloy heating elements ensures fast, uniform heat distribution and minimal thermal overshoot.
  • Infrared CO₂ sensor with automatic zero-point calibration, temperature compensation, and overvoltage/reverse-polarity protection delivers long-term stability and measurement integrity (±0.1% vol accuracy).
  • Integrated UV germicidal lamp (254 nm, ozone-free) disinfects circulating air and humidification pan vapor; optional 90°C humid heat sterilization cycle meets ISO 14644-1 Class 5 cleanroom-compatible decontamination requirements.
  • Reservoir-style stainless steel water pan with large evaporation surface area enables rapid humidity recovery (<3 min to 95% RH post-door opening) and stable saturation across the full chamber volume.
  • Anti-tilt shelf design maintains horizontal alignment even when extended halfway—preventing media spillage during handling.
  • Electropolished mirror-finish 304 stainless steel interior with seamless, radius-cornered construction minimizes microbial harborage and facilitates validated cleaning protocols per GLP/GMP Annex 1.
  • Intelligent control interface features real-time multi-parameter display (temp, CO₂, RH, elapsed time), programmable timer modes (run-time, constant-temp, constant-humidity, or combined), and user-defined alarm thresholds for temperature deviation, low water level, and door-open duration.

Sample Compatibility & Compliance

The ZCQ-50 supports standard T-25, T-75, and multi-well plates, Petri dishes, roller bottles, and flasks used in primary cell isolation, monoclonal antibody development, and regenerative medicine applications. Its HEPA-filtered (≥99.998% @ 0.3 µm) intake system complies with ISO 14644-1 airborne particulate standards for Class 5 environments. The unit conforms to IEC 61010-1:2010 safety requirements for laboratory equipment and supports audit-ready operation through configurable event logging—including door status, temperature excursions, CO₂ setpoint changes, and sterilization cycles—aligning with FDA 21 CFR Part 11 data integrity expectations when paired with optional RS485 interface and external LIMS integration.

Software & Data Management

While the base ZCQ-50 operates via an intuitive LCD interface with non-volatile memory for parameter retention during power interruption, optional upgrades include a color touchscreen controller with USB export capability for CSV-formatted environmental logs. All configurations support timestamped event records (e.g., door open/close, alarm activation, sterilization start/end), enabling retrospective analysis per ALCOA+ principles. When connected via RS485, the incubator integrates with centralized monitoring platforms compliant with ISO/IEC 17025 quality management systems and supports remote verification of operational status without physical access.

Applications

The ZCQ-50 serves as a foundational platform for academic and industrial life science research requiring stringent environmental fidelity: routine maintenance of adherent and suspension cell lines (e.g., HeLa, CHO, HEK293); generation of monoclonal antibodies via hybridoma culture; preimplantation embryo development in assisted reproductive technology (ART); differentiation protocols for induced pluripotent stem cells (iPSCs); cytotoxicity screening in pharmaceutical development; and long-term co-culture studies modeling tumor microenvironments. Its robust performance under variable ambient lab conditions makes it suitable for core facilities, contract research organizations (CROs), and biomanufacturing QC labs operating under ISO 13485 or cGMP frameworks.

FAQ

What is the difference between gas-jacketed and water-jacketed CO₂ incubators?
Gas-jacketed models like the ZCQ-50 use internal air-heating elements for faster temperature recovery and reduced maintenance, whereas water-jacketed units rely on thermal mass from surrounding water—offering greater stability during power loss but requiring periodic water replenishment and microbial monitoring.
Does the ZCQ-50 meet regulatory requirements for GMP-compliant cell culture?
Yes—the instrument’s traceable calibration capabilities, alarm logging, door-event tracking, and optional data export support compliance with EU GMP Annex 1 (Section 8.22), USP , and ISO 13485:2016 clause 7.5.10 for controlled environment documentation.
Can the UV lamp operate while the chamber is in use?
No—UV irradiation is interlocked with door position and chamber temperature; it activates only during dedicated sterilization cycles at ambient or elevated temperatures, preventing phototoxic damage to live cultures.
Is humidity control active during CO₂ purging or door openings?
Yes—the reservoir-based humidification system continuously supplies saturated vapor, and the intelligent control algorithm dynamically adjusts heater duty cycle to maintain 95% RH ±3% RH even during repeated 30-second door events.
What validation support is available for IQ/OQ/PQ protocols?
DRETOP provides factory-assembled calibration certificates for temperature (NIST-traceable PT100 probe), CO₂ (certified gas mixture verification), and humidity (hygrometer reference standard), along with blank protocol templates aligned with ASTM E2500-13 and PDA Technical Report No. 13.

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