Flyer

The ExPERT GTx

Delivery of virtually any molecule, into any cell, at any scale

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 ≥90%.

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.

  • Rapidly transfect from 75 thousand to 20 billion cells
  • 21CFR Part 11 enabled software
  • Established regulatory path supported by FDA master file
  • Closed, cGMP-compliant system
  • MaxCyte’s proprietary Flow Electroporation technology

Features

The ExPERT GTx provides enhancements that improve ease of use, processing workflow, regulatory compliance, and overall user experience with its elegant design that fits seamlessly into any high-tech laboratory space.

Features-icon
  • Integrated touch-screen - easy operation with a touch of a finger
  • Enhanced software user interface - upgraded, 21 CFR Part 11 enabled software provides additional regulatory compliant functionality and intuitive ease of use
  • LED status indicators - six colorful and clearly defined status modes provide the user with a quick way to visualize instrument and run status
  • Barcode reader - capture important sample processing details and minimize manual information entry to improve overall sample, reagent and Processing Assembly traceability
  • Retractable bag hooks - easily available when needed for large volume processing and then fold away when not in use
  • Reduced footprint - industry’s leading transfection processing capacity in a small footprint - maximizes productivity while saving valuable laboratory counter space
  • Elegant design - modern and sleek appearance to enhance laboratory aesthetics

Network capable

  • Shared local drive access to generate and save reports automatically
  • Electronic signatures to minimize transcription errors
  • Network user authentication to reduce the number of passwords needed
  • Application programing interface (API) capable to integrate into your manufacturing automation system

Standard features

  • Flow electroporation capable
  • Static electroporation capable
  • Compatible with all MaxCyte processing assemblies
  • Scalable capabilities from 75 thousand cells to 20 billion cells

Quality and regulatory features

  • 21 CFR Part 11 enabled software
  • FDA master file supported
  • cGMP-compliant system
  • Independently CE tested to comply with the applicable EMC Directive requirements (IEC 61326-1, EN 61000) and safety standards (SPE 1000, EN 61010, CSA 61010-1)
maxcyte-expert-img@2x

Service and support package

  • Provides installation qualification and operational qualification support
  • Provides annual calibration support
  • In-lab support by experienced field applications scientists
  • Global support throughout North America, Europe, Israel, Asia, and Australia

ExPERT GTx instrument specifications

Item Specifications
GTx Instrument Dimensions 8.7” (221mm) x 19.4” (493mm) x 17.6” (448mm)
GTx Instrument Weight 55 lbs (25 Kg)
GTx Input Power 100-240VAC, 50-60Hz, 3.5A
Fuse Requirements 2X 4A Slow Blow, 250V, 5X20mm
Operating Humidity 93% Maximum
Operating Temperature 15°C - 25°C
Storage Temperature 0°C - 45°C
Modes of Operation Static and Flow
Process Volumes 20 µL – 100 mL
Performance (Flow Mode) 8 mL / minute
Ports Available 1 USB / 1 Ethernet

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

Bring the ExPERT GTx to your lab

Ready to transform your research? Our customer support team is ready to build you a quote.