200 cm µPAC™ column
As an alternative to conventional columns, PharmaFluidics offers micromachined nano-LC columns or micro Pillar Array Columns (µPAC™). These µPAC™ columns display exceptional separation properties with unprecedented peak capacity and narrow peak shapes at low operating back-pressure. µPAC™ column, 200 cm length, with pillar array backbone at interpillar distance of 2.5µm, C18.

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Good product that needs a bit more optimization for lot to lot reproducibility.
Proteomics and targeted peptide quantitation
This column has got good potential to be a strong competitor in the field of proteomics. The downside is optimization of LC gradient and long re-equilibration but this is paid off by robustness and peak capacity
Review Date: 14 Nov 2019 | PharmaFluidics
High-performance separation tool for flow rate range between 100nl/min - 1,0µl/min and injection volume range of 4nl up to 5µl; to be used in applications for biomarker discovery (proteomics, metabolomics, lipidomics )and the analysis of biopharmaceuticals. As an alternative to conventional columns, PharmaFluidics offers micromachined nano-LC columns or micro Pillar Array Columns (μPAC™). These μPAC™ columns display exceptional separation properties with unprecedented peak capacity and narrow peak shapes at low operating back-pressure. µPAC™ column, 200 cm length, with pillar array backbone at interpillar distance of 2.5µm, C18.
High-throughput, routine, and comprehensive proteome analysis using a µPAC-based capillary-flow LC-MS workflow
In this application note, PharmaFluidics describes optimal LC methods for a variety of LC-MS based proteome analyses. This application note highlights PharmaFluidics' µPAC™ capLC column as a column that promises to maximize throughput of routine proteome analysis.
Non-targeted host cell protein monitoring in downstream process samples µPAC™-MS
In this application note, PharmaFluidics uses micropillar array columns (µPAC™) in combination with mass spectrometry for the characterization of host cell proteins and their monitoring during downstream processing.
µPAC™ - A New Generation of Micro-Chip Based HPLC Columns
Learn more about µPAC™ micro-Chip based HPLC columns from PharmaFluidics
Sensitive Detection of Peptides in Cytochrome C Digest Using Nano LC
Liquid chromatography coupled with mass spectrometry is a powerful analytical tool for detection and identification of chemicals in complex mixtures. With the low flow capability of Nano LC-MS, higher resolution, ion suppression tolerance and ionisation efficiency is obtained which gives greater chemical sensitivity. The low flow capability of nano-LC couples perfectly with the microfluidics of the Microsaic 4500 MiD® mass detector. The reduced solvent, nitrogen and power consumption of the Microsaic 4500 MiD® provides a lower cost and greener solution for mass detection.
Why Should You Use µPAC™?
Discover 6 key reasons why you should use µPAC™ columns for your your separations.
µPAC™ Column Performance with Peptide Standards
Peptide standards are critical in mass spectrometry based proteomics to ensure optimal and consistent system performance before, during, and after sample analysis. They can be used to assess peptide elution, troubleshoot chromatography, predict retention time, and to demonstrate that the LC-MS platforms are working properly.
μPAC™ Column Robustness in Bottom-Up Proteomics
The Pharmafluidics μPAC™ column's micromachined micro-pillar array technology provides distinct advantages over competitors. In this application note, Pharmafluidics discusses how sharp separation peaks, low backpressure, and resilience that allow the μPAC column to boost laboratory output.
Using the μPAC and Microsiac 4500 MiD for Cytochrome C Peptide Detection
In this application note, Pharmafluidics demonstrates the linkage of the Microsaic 4500 MiD® to the μPAC™ column, producing a compact and high-res platform for separations.
The Role of Perfect Order in LC Micro Pillar Arrays Part 2: Performance in Gradient Separations
In part 2 of this technical note, you will find further analysis of performance and efficiency in the μPACTM column, including peak gain, width, and capacity.
Ceramide Profiling Using an μPAC™ Micro-Array Column Combined with High-Res Mass Spectrometry
Ceramides, a type of sphingolipid, form a key role in skin permeability in the human body. Due to the structural diversity present, profiling ceramides requires high-fidelity chromatographic separation. In this note, the μPAC™ column is used to successfully perform this separation
Exceptional LC-MS Sensitivity and Reproducibility with PharmaFluidics’ New Trapping Column
Ir. Paul Jacobs, COO of PharmaFluidics, discusses its new micropillar array ‘trapping’ column launched at Pittcon 2018. This novel technology complements the already existing analytical column in chromatographic systems to enable higher flow rates, sample enrichment, and sample de-salting. Coupled with state-of-the-art mass spectrometry platforms, the trapping column will bring highly efficient and reproducible biomolecular separation to the user.
How to Connect the µPAC™ Column for Liquid Chromatography: Video Guide
In this video guide, learn how to set-up the µPAC™ column for performing HPLC. The µPAC is compatible with industry standard connections, making setup fast and simple.
The µPAC™ Column: Unprecedented Separation Power with a Compact Form
In this video, discover how the µPAC™’s micromachined separation bed technology produces a miniaturized, high-performance separation tool compatible with all Nano-LC-MS equipment. The µPAC's design makes it ideal for small volumes of complex samples, such as in biomarker identification and biopharmaceutical development.
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New format for PharmaFluidics’ µPAC™ columns to meet surging customer demand
We talk with the team at PharmaFluidics about how their recent changes in sourcing and production allows them to face demand from a growing community of users
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How to Double Your IDs Using Micro Pillar Array Chromatography Columns
Watch this on-demand expert webinar on how to use µPAC™ to improve the sensitivity of single-cell proteomic samples

































