The ExPERT GTx electroporator is capable of high-performance delivery of virtually any molecule, into any cell, at different scales with the unique ability to transfect primary cells, stem cells and cell lines with minimal disturbance resulting in transfection efficiencies routinely at or above 90 percent.

The GTx stands out as the sole enabler of a commercially available, non-viral manufactured advanced therapy medicinal product (ATMP). It showcases the industry’s foremost clinically-validated and scalable electroporation technology, specifically designed for complex cellular engineering.

From product development to translation into clinical trials, GTx’s clinically validated scalable electroporation technology is equipped to handle your most complex cellular engineering demands.

• Rapidly transfect from 75 thousand to 20 billion cells.
• Move forward with 21 CFR Part 11 enabled software.
• Develop quickly with an established regulatory path supported by a FDA Master File.
• Manufacture confidently with closed, cGMP-compliant, ISO-certified and CE-marked products.
• Enjoy MaxCyte’s proprietary Flow ElectroporationⓇ technology.

Consistent, reproducible results – Achieve robust transfection across various donors and manufacturing sites.

Seamless tech transfer – Simplified instrument and processing assembly setup reduce operator-related errors.

Open connectivity to DCS – Seamless real-time integration with Distributed Control Systems (e.g., DeltaV™) for consistent process control, data collection, and improved batch records.

Time synchronization – Unified timestamps across devices for enhanced compliance, data integrity and simpler audits.

Small footprint – Minimize space requirements in the manufacturing suite.

Pre-optimized protocols – Over 80 cell types supported, saving time on electroporation parameter optimization.

Fast processing – 8 mL/min throughput helps maintain cell health.

High cell concentrations – Process 0.5–2×10^8 cells/mL for both autologous and allogeneic workflows.

Scalability: Flexible processing assemblies handle volumes from 15 µL to 100 mL.

Standards to which conformity is declared

• EN61010-1:2010 -3rd Edition: Safety requirements for electrical equipment for measurement, control, and laboratory use Part 1: General requirements
• EN61326-1:2013: Electrical Equipment for Measurement, Control and Laboratory Use – EMC Requirements
• CRISPR 11:2009 +A1:2010: Limits and methods of measurement of electromagnetic disturbance characteristics of industrial, scientific and medical (ISM) radio-frequency equipment
• IMDF/CYBR WG/N 60: Principles and Practices for Medical Device Cybersecurity

CE Marking Application of Council Directive(s):

• 2004/108/EC
• 20014/35/EC