JM Science to Showcase Shiseido HPLC Columns for Protein Separation at Pittcon 2014

11 Dec 2013
Sarah Thomas
Associate Editor

Product news

Chromatographic separations of proteins are based on their difference either in size (size exclusion chromatography), electric charges (ion exchange chromatography), or hydrophobicity (reversed-phase chromatography). JM Science offers a complete line of Shiseido HPLC CAPCELL PAK Columns with the developed Proteonavi to separate proteins and peptides in reversed phase mode. In reversed-phase mode, it is known that proteins and peptides with higher-order structure are denatured to some extent in the course of being retained on the stationary phase after introduction to the column. Once the retention with denaturation is occurred, molecules will not migrate until the organic content of the mobile phase is raised to an appropriate level under a gradient program.

Proteonavi utilizes high-purity silica with few metal impurities, and shows minimal irreversible adsorption for proteins and peptides. Its pore size is as wide as 30 nm, so that large proteins are able to have enough interactions with the stationary phase.

The primary source of protein retention on reversed phase is hydrophobic interaction between hydrophobic parts of amino acids residues and alkyl chains in the stationary phase. When secondary interactions, such as coulombic interactions by acidic silanols or metal impurities in the stationary phase, exist to a large extent, peak shapes of proteins will be deteriorated due to their slow kinetics. Proteonavi shows better peak profiles and higher resolution among standard proteins, in comparison with conventional wide-pore columns.

Proteonavi is suitable to large-scale preparative separation, taking advantage of its low-column bleed nature and high separation efficiency.

JM Science will be exhibiting these new HPLC CAPCELL PAK Columns at PITTCON 2014 at Booth# 2802.

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UHPLC and HPLCHigh performance liquid chromatography (HPLC) and ultra high performance liquid chromatography (UHPLC), also known as UPLC, are analytical techniques used to separate, identify and quantitate components of complex mixtures including biological samples such as proteins and lipids as well as chemical mixtures of pesticides, drugs and oils. Both techniques are liquid chromatographic methods but differ by operating pressures (HPLC < 6000 psi < UHPLC ). Components of HPLC and UHPLC systems include columns, detectors, pumps, autosamplers and column heaters. Explore a range of UHPLC and HPLC columns for your specific sample needs including reverse phase, normal phase, ion exchange, HILIC, ion exclusion and size exclusion columns. For more specialized HPLC, explore FPLC, countercurrent LC and simulated moving bed systems. Find the best UHPLC and HPLC equipment in our peer reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.ProteomicsProteomics is the systemic bioinformatics study of proteins and amino acids, including their structure, size, function and identification. Tools used in proteomics include chromatography, blotting and gels, protein arrays, mass spectrometry and ELISA and associated analysis software. Analyzers and proteomic systems should be sensitive, high resolution, fast and may be automated for high-throughput.PittconPittcon is one of the largest conferences and exhibitions dedicated to laboratory science. It brings together professionals and innovators in analytical chemistry, physics, and biology, offering a platform to explore the latest scientific tools and technologies. From cutting-edge laboratory instruments to emerging research trends, Pittcon is a must-attend event for professionals in research and development. Protein BiologyThe analysis of protein expression, identity and function is vital for many areas of life science research and drug discovery. Some of the most commonly used techniques in protein analysis include Western blotting, electrophoresis and mass spectrometry.
JM Science to Showcase Shiseido HPLC Columns for Protein Separation at Pittcon 2014