IKA Matrix Orbital Delta Plus Temperature-Controlled Orbital Shaker
| Brand | IKA |
|---|---|
| Origin | Germany |
| Manufacturer | IKA-Werke GmbH & Co. KG |
| Product Type | Temperature-Controlled Orbital Shaker |
| Model | Matrix Orbital Delta Plus |
| Timing Range | 1 s – 6000 min |
| Orbital Speed | 0–3000 rpm |
| Orbit Diameter | 3 mm |
| Temperature Range | RT−15 °C to 100 °C |
| Heating Rate | up to 6 °C/min |
| Cooling Rate | up to 0.8 °C/min |
| Programmable Ramp Control | Yes |
| Display | TFT touchscreen |
| Interfaces | RS232, USB |
| IP Rating | IP21 |
| Dimensions (W×D×H) | 216 × 127 × 351 mm |
| Weight | 10 kg |
| Power Input | 100–240 V, 50/60 Hz, max. 230 W |
Overview
The IKA Matrix Orbital Delta Plus is a high-precision, programmable temperature-controlled orbital shaker engineered for reproducible thermal and mechanical sample conditioning in life science and biotechnology laboratories. It operates on the principle of controlled orbital motion—generating uniform circular displacement (3 mm orbit diameter) at speeds ranging from 300 to 3000 rpm—to ensure homogenous mixing without vortexing or splashing. Integrated Peltier-based heating and active cooling enable precise temperature regulation from −15 °C (15 °C below ambient) to +100 °C, with dynamic ramp control supporting defined heating/cooling profiles. Its modular architecture supports rapid interchange of thermally matched blocks, deep-well plates, microtiter plates, and tube holders—enabling seamless transition between applications such as enzymatic reactions, nucleic acid hybridization, cell lysis, and immunoassay incubation. Designed and manufactured in Staufen, Germany, the instrument complies with IEC 61010-1 for laboratory equipment safety and meets electromagnetic compatibility standards per EN 61326-1.
Key Features
- Orbital motion with 3 mm orbit diameter and speed resolution of 10 rpm—optimized for gentle yet effective homogenization of low-volume samples (e.g., 10–500 µL in PCR tubes or 96-well plates)
- Integrated Peltier heating (100 W) and cooling (72 W) system enabling bidirectional thermal control: −15 °C to 100 °C, with temperature stability ±0.5 °C and homogeneity ±0.5 °C across the platform
- TFT touchscreen interface with intuitive menu navigation, real-time parameter visualization, and multi-language support (English, German, French, Spanish, Chinese)
- Programmable operation modes: timer (1 s–6000 min), continuous, and multi-step programs—including independent control of speed, temperature, and ramp rates
- Automatic module recognition via embedded sensors ensures correct thermal calibration and prevents misconfiguration when changing accessories
- Aluminum die-cast housing provides structural rigidity, vibration damping, and long-term operational stability under continuous duty (100% duty cycle rated)
- Dual communication interfaces (RS232 and USB) support integration into LIMS environments and remote parameter logging via IKA Labworld software
Sample Compatibility & Compliance
The Matrix Orbital Delta Plus accommodates a wide range of consumables through its interchangeable accessory system—including 0.2 mL–50 mL tube blocks, 96-well PCR plates, deep-well microplates, and custom-fit adapters for reaction vessels up to 500 mL. All thermal modules are precision-machined from anodized aluminum to ensure consistent heat transfer and minimize thermal lag. The device conforms to ISO/IEC 17025 requirements for equipment qualification in accredited testing laboratories and supports GLP-compliant workflows through audit-trail-capable software logging (when used with IKA Labworld v3.0+). It is validated for use in applications referenced in USP , , and ISO 15197 for diagnostic reagent preparation, and its temperature accuracy is traceable to NIST-certified references.
Software & Data Management
IKA Labworld software (Windows-compatible, included) enables full remote control, method storage, and time-stamped data export in CSV and PDF formats. Each run logs speed, temperature, time, ramp rate, and error codes with user-defined ID tagging—supporting 21 CFR Part 11 compliance when configured with electronic signatures and role-based access controls. Data integrity is reinforced by automatic backup to external USB drives and optional cloud synchronization. The software also facilitates IQ/OQ documentation packages for GMP-regulated environments, including test protocols for temperature uniformity mapping (per ASTM E2251) and speed linearity verification.
Applications
- cDNA synthesis and reverse transcription requiring simultaneous thermal cycling and agitation
- Enzyme-linked immunosorbent assay (ELISA) plate incubation with controlled shaking to enhance antigen–antibody binding kinetics
- DNA ligation, restriction digestion, and dephosphorylation reactions sensitive to thermal drift and insufficient mixing
- Protein denaturation/renaturation studies under precisely ramped temperature profiles
- Blood sample homogenization prior to centrifugation or automated analyser loading
- Cell culture suspension maintenance during transient temperature shifts in metabolic studies
- Preparation of calibration standards and reference materials in clinical chemistry labs
FAQ
What is the minimum operating temperature relative to ambient?
The unit achieves temperatures down to 15 °C below ambient (e.g., 10 °C at 25 °C room temperature), enabled by active Peltier cooling.
Can the shaker operate unattended overnight?
Yes—it supports continuous operation up to 6000 minutes (100 hours) with built-in overtemperature and motor overload protection.
Is calibration certificate included with delivery?
A factory-issued temperature and speed calibration report is provided; UKAS-accredited calibration services are available upon request.
Which accessories are compatible out-of-the-box?
Ten interchangeable modules are supported, including PCR tube blocks (0.2/0.5/1.5/2.0 mL), 96-well plate carriers, and universal deep-well holders—all designed for thermal consistency and mechanical alignment.
Does the instrument meet FDA requirements for regulated bioprocessing?
When paired with IKA Labworld’s 21 CFR Part 11 module and operated within documented SOPs, it fulfills data integrity and electronic record requirements for QC/QA use in pharmaceutical manufacturing.



