OverviewThe CellCelector CLD is an automated cell imaging and isolation platform designed for cell line development (CLD) workflows. It integrates high-sensitivity brightfield and optional multi-channel fluorescence imaging with automated single-cell and colony picking to support high-throughput clone screening, monoclonality documentation and downstream expansion.
Why CellCelector CLD- Accelerates clone screening and productivity assessment with high-speed scanning and intelligent imaging
- Detects low-expression targets with enhanced sensitivity and shading correction
- Provides audit-ready image and metadata documentation for regulatory traceability
- Enables high transfer efficiency and viability for reliable downstream expansion
How it works- Seed candidate pools into Next Generation CLD Nanowell Plates to maximize single-cell occupancy and minimize cross-contamination
- Perform automated brightfield imaging and segmentation to identify single-cell nanowells and exclude multicell wells
- Track lineage and clonal expansion across timepoints to document monoclonality
- Use optional fluorescence channels to quantify secretion/binding and enable multiplexed productivity ranking
- Isolate and transfer top clones with a gentle single-cell picking arm preserving viability
- Automatically capture images and metadata (plate maps, timestamps, analysis masks, decision criteria) for audit-ready records
Key features and product highlights- High-content imaging with dual objectives (4× for wide-field scanning, 10× for verification)
- Optional five-channel fluorescence unit for marker-based selection and quantitative ranking
- Next Generation CLD Nanowell Plates: screening up to 85,000 candidate clones per plate
- Single-use 80 µm glass capillary for gentle, high-precision nanoliter aspiration
- Heated deck tray to maintain stable 37°C conditions during operations
- Single curved frameless monitor station for consolidated image, metadata and table views
- Maintenance-free design to reduce routine downtime
- Automated documentation and traceable audit trails to support clonality evidence
Performance and claimed benefits- Reported transfer efficiency and viability up to 100% for retrieved cells
- Screening throughput up to 85,000 candidate clones per Next Generation CLD Nanowell Plate
- Demonstrated ~40% more monoclonal wells and >3× higher clone outgrowth versus standard plates in comparative tests
- Rapid identification of top clones from large candidate pools for faster downstream development
Applications and target users- Bioprocess and CLD teams scaling antibody and recombinant protein production
- Research and development labs prioritizing throughput, reproducibility and documented clonality
- Programs working with low-expression targets requiring sensitive imaging and multiplex screening
Example data and resources (descriptive)Provided example workflows and screens include Day 4 productivity assays (brightfield, false-color and fluorescence channels), imaging and growth screenshots that illustrate monoclonality verification and pick-readiness metrics.
Technical specifications- Model: CellCelector CLD (automated imaging and single-cell/colony picking platform)
- Optional fluorescence: up to five channels for marker-based selection and quantitative ranking
- Microscope objectives: 4× (wide-field scanning) and 10× (high-resolution verification)
- Picking capillary: 80 µm single-use glass capillary for nanoliter aspiration
- Deck temperature control: heated deck tray to maintain 37°C during operations
- Nanowell plate capacity: supports screening up to 85,000 candidate clones per plate
- Imaging enhancements: shading correction algorithm and advanced sensitivity for low-expression targets
- Transfer performance: up to 100% transfer efficiency and viability (reported)
- Operation: maintenance-free daily operation to reduce downtime
- Documentation: automated image and metadata capture (plate maps, timestamps, analysis masks, decision criteria)
- Demonstrated cell types: CHO (including CHO K1), HEK293, hybridoma; plate coatings available for ultra-low attachment and plasma coatings to support iPSC and cancer cell lines