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AssayMAP Bravo Protein Sample Prep Platform

Easy, proven and scalable automated protein and peptide sample preparation

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Agilent Technologies

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Average Rating 5.0

|1Scientists have reviewed this product

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Highly recommended as alternative to bead-based immunoaffinity enrichment workflows.

 

Average Rating 5.0

Application Area:

Proteomics & peptidomics sample preparation; immunoaffinity enrichment and purification

This is an extremely easy system to use. We added this tool to our collection to supplement a magnetic-bead based workflow with a tip based workflow. Much faster, uses less consumables and nice to have a walk-away platform where you can focus on other things while the robot does all the work!

Review Date: 19 Jul 2021 | Agilent Technologies

The AssayMAP Bravo microchromatography platform combines the precision high-throughput liquid handling of the Agilent Bravo with the AssayMAP microchromatography technology. The heart of the AssayMAP technology is comprised of packed-resin bed microchromatography cartridges, positive-displacement syringes, and pre-optimized applications.

AssayMAP cartridges are manufactured with rigorous quality control to exacting specifications and are available in 2 sizes (standard and large-capacity) with diverse media chemistries to meet your specific workflow needs. Purified proteins, peptides, and enriched molecules can be directly used in downstream analyses such as LC/MS, binding studies, or activity assays.

  • Intuitive software with pre-optimized protocols for quick setup and run execution
  • Proven and reliable platform with over 175 peer-reviewed publications
  • Scalable, process from 8 to 96 samples in parallel
  • Reproducible sample preparation enables consistent results from operator-to-operator, simple workflow transfers between labs, and scientists to get the best results possible from downstream analytical instruments.
  • Consistent and quantitative yields enable confident decisions with fewer replicates
  • VWorks Plus software enables compliance with electronic record integrity requirements such as US FDA 21 CFR, Part 11 or EU Annex 11.

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