Literature DB >> 19959987

Using the GELFREE 8100 Fractionation System for molecular weight-based fractionation with liquid phase recovery.

Chuck Witkowski1, Jay Harkins.   

Abstract

The GELFREE 8100 Fractionation System is a novel protein fractionation system designed to maximize protein recovery during molecular weight based fractionation. The system is comprised of single-use, 8-sample capacity cartridges and a benchtop GELFREE Fractionation Instrument. During separation, a constant voltage is applied between the anode and cathode reservoirs, and each protein mixture is electrophoretically driven from a loading chamber into a specially designed gel column gel. Proteins are concentrated into a tight band in a stacking gel, and separated based on their respective electrophoretic mobilities in a resolving gel. As proteins elute from the column, they are trapped and concentrated in liquid phase in the collection chamber, free of the gel. The instrument is then paused at specific time intervals, and fractions are collected using a pipette. This process is repeated until all desired fractions have been collected. If fewer than 8 samples are run on a cartridge, any unused chambers can be used in subsequent separations. This novel technology facilitates the quick and simple separation of up to 8 complex protein mixtures simultaneously, and offers several advantages when compared to previously available fractionation methods. This system is capable of fractionating up to 1mg of total protein per channel, for a total of 8 mg per cartridge. Intact proteins over a broad mass range are separated on the basis of molecular weight, retaining important physiochemical properties of the analyte. The liquid phase entrapment provides for high recovery while eliminating the need for band or spot cutting, making the fractionation process highly reproducible.

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Year:  2009        PMID: 19959987      PMCID: PMC3152241          DOI: 10.3791/1842

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  1 in total

1.  Multiplexed size separation of intact proteins in solution phase for mass spectrometry.

Authors:  John C Tran; Alan A Doucette
Journal:  Anal Chem       Date:  2009-08-01       Impact factor: 6.986

  1 in total
  4 in total

1.  Robust two-dimensional separation of intact proteins for bottom-up tandem mass spectrometry of the human CSF proteome.

Authors:  Adriana Bora; Carol Anderson; Muznabanu Bachani; Avindra Nath; Robert J Cotter
Journal:  J Proteome Res       Date:  2012-05-11       Impact factor: 4.466

2.  Optimization of protein-level tandem mass tag (TMT) labeling conditions in complex samples with top-down proteomics.

Authors:  Yanting Guo; Dahang Yu; Kellye A Cupp-Sutton; Xiaowen Liu; Si Wu
Journal:  Anal Chim Acta       Date:  2022-06-07       Impact factor: 6.911

3.  Plasma proteome analysis on cynomolgus monkey (Macaca fascicularis) pedigrees with early onset drusen formation.

Authors:  Hiroaki Kobayashi; Haru Okamoto; Akira Murakami; Takeshi Iwata
Journal:  Exp Anim       Date:  2014

4.  Comparative proteomic analysis of different stages of breast cancer tissues using ultra high performance liquid chromatography tandem mass spectrometer.

Authors:  Abdullah Saleh Al-Wajeeh; Salizawati Muhamad Salhimi; Majed Ahmed Al-Mansoub; Imran Abdul Khalid; Thomas Michael Harvey; Aishah Latiff; Mohd Nazri Ismail
Journal:  PLoS One       Date:  2020-01-16       Impact factor: 3.240

  4 in total

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