What is the primary benefit of a single-use chromatography system?

The main benefit is the elimination of cleaning and cleaning validation between runs, which reduces downtime, minimises cross-contamination risk, and simplifies GMP compliance.

Can this system be used for different purification methods?

Yes, ÄKTA ready systems are typically flexible and can be configured for various purification needs, including isocratic and gradient elution, with options for variable UV detection.

Is this equipment suitable for GMP environments?

Units of this type are specifically designed and documented to support GMP-regulated biopharmaceutical production, including extensive regulatory support.

What kind of consumables does this system use?

It uses proprietary single-use disposable flow paths and associated components, which are replaced between batches to ensure sterility and prevent cross-contamination.

How scalable is the ÄKTA ready platform?

The platform is designed for scalability, with different flow kits supporting a wide range of process volumes, from small-batch purification to larger process requirements when paired with larger models.

used Equipment

Available

Verified seller

Cytiva Sweden AB - AKTA Ready Chromatography System

Name: AKTA Ready Chromatography System
Brand: Cytiva Sweden AB
SKU: 1696171. MOB102
Availability: InStock

Price: Contact seller for price

This listing is for an ÄKTA ready™ Chromatography System

The unit is in full working condition and is ready for immediate release

The ÄKTA ready™ Chromatography System is a single‑use liquid chromatography platform engineered for bioprocessing, process scale‑up, and GMP‑regulated manufacturing of biologics, including monoclonal antibodies, recombinant proteins, viral vectors, nucleic acids, and other sensitive therapeutic products.

Key Characteristics

Single‑use disposable flow paths — eliminate the need for cleaning and cleaning validation between runs, reduce downtime, and minimize cross‑contamination risk.
Flexible operation — available in multiple configurations (isocratic, gradient, variable UV, extended) to match different purification needs.
Scalable platform — flow kits for low and high flow rates support a wide range of process volumes; systems scale from small‑batch purification to larger process requirements when paired with larger ÄKTA ready™ XL models.
Designed for GMP environments — extensive documentation and regulatory support help meet compliance demands in regulated biopharmaceutical production

Cambridgeshire, United Kingdom

5,791 km away

Model Number

Chromatography System

Stock Number

1696171. MOB102

Machinery Masters View

Typical context for this category of equipment. Always confirm specifics with the seller.

Applications & Use Cases

Biopharmaceutical manufacturing, particularly for monoclonal antibodies and recombinant proteins.
Viral vector and nucleic acid purification in gene therapy and vaccine production.
Process scale-up and development for new biological entities.
GMP-regulated manufacturing environments requiring high purity and minimal cross-contamination.
Production of sensitive therapeutic products where single-use technology is advantageous.

Typical Specifications

Typical flow rate range: Units in this class commonly offer flow rates from tens of millilitres per minute up to several litres per minute, depending on the flow kit installed.
Operating pressure: Typically designed for pressures suitable for process-scale chromatography, often up to 0.5 MPa (5 bar).
Power supply: Commonly requires a standard industrial single-phase supply, typically 100-240 VAC, 50/60 Hz.
Footprint: For this class of equipment, units are designed for integration into bioprocessing suites, with a footprint that can vary based on configuration but is generally compact for its capacity.
Material compatibility: The single-use flow paths are typically constructed from biocompatible plastics, such as polypropylene and polyethylene, suitable for pharmaceutical contact.
Control system: Units of this type are typically controlled via integrated software, offering comprehensive method development and run control.
Maintenance requirements: Due to single-use flow paths, routine cleaning and cleaning validation are eliminated, significantly reducing maintenance related to product contact parts.

Frequently Asked Questions

The main benefit is the elimination of cleaning and cleaning validation between runs, which reduces downtime, minimises cross-contamination risk, and simplifies GMP compliance.

Machinery Masters Intelligence. General guidance for this category of equipment only, not a substitute for the seller's exact specifications. Always confirm details with the seller.