Products & ReviewSeparations

50 cm µPAC™ column

PharmaFluidicsCOL-nano050G1BAvailable: Worldwide

With an internal volume of 3µL, this 50 cm long RP-C18 µPAC™ column is perfectly suited to perform high throughput analyses with shorter gradi­ent solvent times (30, 60 and 90-minute gradients) and it can be used over a wide range of flow rates, between 100 and 2000 nL/min. µPAC™ column, 50 cm length, with pillar array backbone at interpillar distance of 2.5µm, C18.

PharmaFluidics

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Description

High-performance separation tool for flow rate range between 100nl/min - 1,5µl/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. With an internal volume of 3μL, this 50 cm long RP-C18 μPAC™ column is perfectly suited to perform high throughput analyses with shorter gradi¬ent solvent times (30, 60 and 90-minute gradients) and it can be used over a wide range of flow rates, between 100 and 2000 nL/min. µPAC™ column, 50 cm length, with pillar array backbone at interpillar distance of 2.5µm, C18.




Application NoteSeparations

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.


Application NoteSeparations

Routine Proteome Analysis Using 50 cm µPAC™ Columns

The practice of bottom-up proteomics relies to a large extent on the separation performance that can be achieved with state-of-the art nano LC-MS/MS equipment. Depending on the sample complexity or the instrument time that can be dedicated to a certain sample, different LC columns and corresponding LC-MS/MS methods are often required. When aiming for comprehensive proteome analysis with deep coverage, relatively long columns (lengths up to 75 cm) are typically operated with long and shallow solvent gradients, delivering the highest chromatographic performance. This is indeed a good strategy if very complex samples need to be analyzed and when as much information as possible needs to be retrieved from these samples. However, daily routine proteome analysis often deals with much less complex samples or demands increased sample throughput, making total analysis times above 120 min undesirable or even impossible.



Application NoteSeparations

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.




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.



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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