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DispenCell – Single-Cell Dispenser

Compact, automated cell dispenser for fast, easy and gentle single-cell isolation

A simple single-cell dispenser for proof of monoclonality

The DispenCell™ Single-Cell Dispenser is an automated laboratory instrument designed for fast, easy and gentle single-cell isolation. DispenCell integrates seamlessly into your laboratory workflow, with a plug-and-play approach. Flexible and effortless, DispenCell operates equally under sterile conditions in a culture hood, or on a simple benchtop.

Immediate and traceable proof of clonality

DispenSoft, the single-cell analysis software included with DispenCell, provides immediate and traceable proof of clonality. The instrument is fitted with a sensing tip that detects the passage of cells, allowing users to check for proof of clonality immediately after the cells are dispensed. All dispensing data is automatically stored, allowing for easy generation of a clonality report.

Asgentle as manual pipetting

DispenCell has unique technology which allows for extremely gentle handling of the cell sample. Cells are exposed to no more pressure than with manual pipetting (less than 0.2 psi). This allows the instrument to preserve cell viability and outgrowth while simultaneously increasing cell deposition efficiency.

Compact

The small footprint of the DispenCell allows it to fit perfectly into any laboratory setting: under a hood to work under sterile conditions, on a bench top for routine seeding, or in a pre-existing automated workflow.

Verify monoclonality confidently at day zero with a DispenCell and CloneSelect Imager FL bundle

The manual screening methods traditionally used for cell line development are time-consuming and labor-intensive, creating a great demand for high throughput, automated solutions for such efforts. The general workflow below helps identify the systems that can aid in your research.

DispenCell and CloneSelect Imager FL bundle

General specifications
Power Supply External, PSGE120-12-01, 12v, 10A, 120W
Plate holder 2 plates (96 or 384 wells)
Minimal cell number 100 cells
Calibration Not required
Cleaning Not required
Sample prep. 10 min
Cell parameters Size, doublets
Input voltage (External power supply) 100 – 240 V~, 50 – 60 Hz
Input current (External power supply) max 2.0 A
Input voltage (Instrument) 12.0 V
Max. power (Instrument) 36 w
Well plates compatibility 96 WP, 200µL, (655101, Greiner) 384 WP, 50µL, (781101, Greiner) 384 WP low volume, 10µL, (788096, Greiner)
Loading volume per 30s load. time @2×10^⁴ cells/mL : 10µL, 200 cells
Particle range detection capability Dielectric, from 8µm to 25µm
Time to dispense a 96 well plate <= 10 min (provided Tcc < 4s) <= 13 min (provided Tcc < 6s)
Time to dispense a 384 well plate <= 40 min (provided Tcc < 4s) <= 52 min (provided Tcc < 6s)
Monoclonality reliability* >=90%
Missed/Corrupted data points < 1% per plate (only accounted for point serie n>6)
Compressed Air Specifications
Minimum operating pressure Less than 0.2 psi
Instrumentation
Instrument weight 11 kg
Instrument Size 328 x 258.5 x 324.83 mm

Proof of clonality

A single-cell analysis software tool provides a traceable proof of clonality report instantly.

Contamination-free

A patented disposable tip ensures clean isolation of single cells and no cross contamination. Certified free from animal products and cytotoxic material.

High cloning efficiency

Unique design ensures gentle dispensing for better viability and cloning efficiency

Easy to use

Easy to set up, and intuitive with a simple interface. No cleaning or calibration required.

Cell Line Development

Cell Line Development generating biopharmaceutical molecules

Cell line development is a critical step in the process of generating biopharmaceutical molecules, such as monoclonal antibodies. The process often begins with transfecting the host cell type with the DNA encoding the therapeutic protein of interest allowing for random or directed integration of target DNA into the host cell genome. Thousands of clones are screened to isolate the rare high producing cells, a manual and time-consuming process.

Drug Discovery & Development

Drug Discovery & Development Process

For every drug that makes it to the finish line, another nine don’t succeed. This alarming failure rate can be traced to reliance on 2D cell cultures that don’t closely mimic complex human biology, often leading to inaccurate predictions of a drug’s potential and extended drug development timelines.

Monoclonal Antibodies (mAbs)

Monoclonal Antibodies (mAbs)

Monoclonal antibodies (mAbs) originate from one unique parent cell, thus binding only to a single epitope. Monoclonal antibody discovery typically refers to the screening and identification of specific antibodies that target a specific epitope for the diagnosis and treatment of diseases, like the coronavirus for COVID-19.

Monoclonality

Cell line development and assurance of monoclonality

Cell line development and assurance of monoclonality are critical steps in the process of generating biopharmaceutical molecules, such as monoclonal antibodies. A cell line can be established following the isolation of a single viable cell robustly expressing the protein of interest. A key milestone in this process is documenting evidence of clonality. Documentation of clonality is typically image-based, whereby an image of a single cell is produced and included in regulatory filings.