Elite500 Bundle
Automate the most demanding organoid workflows inside a fully enclosed Class II biosafety cabinet. PrecisionOne Elite500 combines preloaded BioApps, intelligent automation, and a protected research environment into a turnkey platform designed for laboratories working with sensitive, infectious, or regulated biological materials.
PrecisionOne automates every step of the single-cell workflow, eliminating manual bottlenecks while improving reproducibility, cell viability, and confidence in every experiment.
Turnkey Single Cell Dispensing for Protected Research
Class II Biosafety Cabinet | Single Cell Dispensing | Integrated Incubators | Integrated Imaging | No Programming
What's Included?
The PrecisionOne Bundle is designed for simplicity. Ready to go out of the box, already programmed to do the workflows you need, and the tools to do them with. Built for you. Built for your automation.
Six-axis intelligent automation platform with integrated machine vision, adaptive calibration and automated tool changing.
Purpose-built applications that automate the most common organoid workflows. Ready to run immediately.
Turnkey Installation
Your system arrives configured, validated, and ready to automate organoid workflows with minimal setup.
Six BioApps. Endless Research Potential.
Dispense Single Cells
Accurately isolate and dispense individual cells into multiwell plates with high repeatability while preserving cell viability.
Verify Clonality
Document monoclonality with built-in verification workflows that improve confidence in downstream research.
Expand Clones
Automate clonal expansion to reduce manual handling and
improve reproducibility.
Passage Cells
Transfer cells consistently between culture vessels with standardized
automated workflows.
Prepare Assay Plates
Automatically dispense media and reagents to prepare plates for downstream single-cell assays.
Plate Cells
Seed cells accurately for reliable well-to-well consistency.
Safely Automate Complex Research
✔ Biosafety Cabinet
✔ Eight-channel Pipette
✔ Plate Handling
✔ Temperature Controlled Media
✔ High Throughput
✔ Automated Scheduling
Seamlessly Connect Your Lab
✔ Benchtop Incubators
✔ BioStorageBot HIVE
✔ LiCONiC Incubators
✔ Molecular Devices Imagers
✔ Leica
✔ Zeiss
✔ Yokogawa
Powered by BioAssemblyBot® 500
At the core of every PrecisionOne™ Elite500 is the BioAssemblyBot® 500, a six-axis intelligent automation platform integrated inside a Class II biosafety cabinet. Designed for laboratories requiring both advanced automation and biological containment, the system combines machine vision, adaptive calibration, automated tool changing, and precision liquid handling within a HEPA-filtered environment that protects researchers, biological samples, and the surrounding laboratory. Supporting up to eight interchangeable BioAssemblyBot Hands, Elite500 automates complex, multi-step workflows while maintaining sterile operating conditions for sensitive or hazardous biological materials.
Technical Specs:
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Integrated Class II Biosafety Cabinet
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Personnel, Product & Environmental Protection
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HEPA-Filtered Work Zone
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Enclosed Sterile Workspace
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Designed for Sensitive & Hazardous Materials
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Six-axis Intelligent Robotic Arm
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Temperature Controlled Media Blocks
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Integrated HD Camera
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HEPA Optional
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UL Certified
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65"W X 33"D X 76"H
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Cell & Gene Therapy
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Patient-Derived Cell Research
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Monoclonal Cell Line Development
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Antibody Discovery
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Vaccine Development
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Regulated Laboratory Workflows
Built for High-Containment Research
Features & Benefits
Class II Biosafety
Ready To Run
Protected Workflows
No Programming
HEPA Filtration
Regulated Research
Ready to Transform Your Workflow?
Book a demo or get a quote:
The BioAssemblyBot 500 is certified by UL in accordance with applicable safety requirements. The BioAssemblyBot 400 is certified by UL in accordance with applicable energy efficiency requirements.
The Advanced Solutions Louisville, KY facility has been audited by UL Registrar LLC and meets GMP requirements listed in RCP, NBCP, or Pharmaceutical Certification Schemes which is uniquely accredited by the American National Standard Institute (ANSI) developed in accordance with applicable sections of the FDA’s code of federal regulations.