The Accellix Instrument | Automated Flow Cytometry

Cell Phenotyping Platform for Automated QC Analytics

The Accellix platform has been adopted by leading immunotherapy companies as it enables standardized and streamlined cytometry of cell therapy drug products.

Small footprint bench-top platform

Manufacturing suite compatible fan-less operation

Simple plug & play installation

Minimal maintenance and no calibration

1 hour setup and operator training

Accellix Instrument

The Accellix Automated Cell Phenotyping Platform is an automated bench-top flow cytometer that leverages a microfluidic cartridge with ambient-stable reagents.

Portable, easy to use, minimal maintenance
Minimal operator training
Fluorescence detection range 510-800 nm
In-run compensation for spectral spillover
No calibration by operator needed

Accellix Software

The Accellix Software is a simple user interface combined with algorithm based autoanalysis software tools which compute a test result at the end of the run. Complete automated analysis increases reproducibility, eliminates subjectivity and simplifies system operation. The Accellix algorithm based autoanalysis software is an algorithm-based analysis tool that automates flow cytometry data analysis using a dynamic gating strategy. It takes in flow cytometry data generated on the Accellix Platform, automatically defines cell subsets, and reports cell population frequencies to users on-screen.

Touchscreen interface with customizable features
On-board computer executes protocol
Instrument delivers both automated results and raw data for manual analysis
Algorithm based autoanalysis results displayed on screen and files generated at protocol conclusion
Ensures traceability-compatible with 21 CFR part 11
The instrument automatically connects to customer's data base through LIMS or similar network

Accellix Optical Path and Spectral Flow

The Accellix Platform is based on spectral flow cytometry. Spectral flow cytometry uses lasers and detectors to capture the entire spectrum of light emitted by fluorescent probes, which enables simultaneous analysis of multiple parameters in a single experiment. The Accellix platform uses a single 488 nm laser diode and a multichannel silicon photomultiplier detector array instead of a standard PMT, adding simplicity, stability, and alignment between platforms.

The advantages of Accellix utilizing spectral flow include:

Stable fluorescence and forward scatter detection

No calibration or compensation needed

No gain adjustments required

Automatic spectral unmixing

6-color panels with single blue laser

What is Flow Cytometry?

Flow cytometry is a powerful analytical technique for analyzing and quantifying cellular populations based on their optical properties and involves passing cells or particles in a fluid suspension through a laser beam, exciting the cells to emit fluorescence. The emitted fluorescence is then detected and measured by a series of detectors and analyzed by software.

The cells are labeled with fluorescent probes that selectively bind to specific cellular components, allowing researchers to distinguish and quantify different types of cells or particles. The technique can be used to measure various characteristics of cells.

Flow cytometry is generally used in research and clinical settings for a wide range of applications such as immunology, cancer research and drug discovery, and is particularly useful for analyzing large populations of cells quickly and accurately, as well as for identifying rare cells within a sample.

In traditional flow cytometry, fluorochromes are excited by a single laser source, and their emission spectra are detected by a limited number of detectors, which limits the number of parameters that can be analyzed simultaneously. Spectral flow cytometry overcomes this limitation by using lasers and detectors, which can measure a wider range of fluorescence spectra, and provides more precise and accurate measurements of fluorescence intensity.

Spectral flow cytometry has several advantages over traditional flow cytometry, including improved resolution and sensitivity, higher spectral resolution, and increased multiplexing capabilities. Spectral cytometers will unmix each spectrum to provide a pure signal for each fluorochrome. A conventional or traditional flow cytometer, while also utilizing lasers as the light source, requires multiple filters and detectors. These filter/detector combinations have a narrow range of detection, which results in a high degree of spillover and therefore use compensation to correct this spillover.