izedquantificationof individualproteins,providesa sensitive and accurate approach to detection of small differencesin the proteinpattern.As an extensionof “oue, ” a data base system for the analysis of two-dimensionalelectrophoretic gels,we reporthere on a screeningalgorithmfordetectionof certainpost-translationalmodificationevents. It is based on the assumptionthat, if there is a post-translationalmodifica-tion of a protein in the transition between two functional statesof a biologicalsystem, in manycasesthesumof the proteinconcentrationof a precursor-productpair in one is equivalentto that in the other. In additionto the identification of candidate pairs with a precursor-product relationship, cues to the nature of the post-translationalmo...
<p>Proteins are represented by protein type, allergen name, number of spots found and number of isoa...
<p>(A) Representative 2D-DIGE gel. Protein extracts from promastigotes of three independent biologic...
Comparing different proteomes by classical two-dimensional electrophoresis is challenging and often ...
<p>Displayed are the analysed protein spots from 2D gel electrophoresis (sample), the probable prote...
After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual ...
AbstractNowadays, investigators in all fields are faced with the identification of unknown, up- or d...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
The study of human protein polymorphism presents a major advantage in clinical chemistry to discover...
The rapid growth of proteomics has been made possible by the development of reproducible 2D gels and...
<p>Proteins were isolated from total protein of MSCs loaded onto the 2-DE gel electrophoresis. First...
Two-dimensional gel electrophoresis is a biochemical technique that combines isoelectric focusing an...
Two-dimensional electrophoresis in polyacrylamide gel provides a highly reproducible display of bios...
*<p>Note: Discrepancy in the isoelectric point (pI) or molecular weight (MW) of the proteins detecte...
<p>A. 2DE gel images of control (up) and ISO-CAs (down) with proteins of interest annotated. B. Enla...
The strategies and methods used by the QUEST system for two-dimensional gel analysis are described, ...
<p>Proteins are represented by protein type, allergen name, number of spots found and number of isoa...
<p>(A) Representative 2D-DIGE gel. Protein extracts from promastigotes of three independent biologic...
Comparing different proteomes by classical two-dimensional electrophoresis is challenging and often ...
<p>Displayed are the analysed protein spots from 2D gel electrophoresis (sample), the probable prote...
After separation through two-dimensional gel electrophoresis (2-DE), several hundreds of individual ...
AbstractNowadays, investigators in all fields are faced with the identification of unknown, up- or d...
International audienceTwo-dimensional gel electrophoresis has been instrumental in the development o...
The study of human protein polymorphism presents a major advantage in clinical chemistry to discover...
The rapid growth of proteomics has been made possible by the development of reproducible 2D gels and...
<p>Proteins were isolated from total protein of MSCs loaded onto the 2-DE gel electrophoresis. First...
Two-dimensional gel electrophoresis is a biochemical technique that combines isoelectric focusing an...
Two-dimensional electrophoresis in polyacrylamide gel provides a highly reproducible display of bios...
*<p>Note: Discrepancy in the isoelectric point (pI) or molecular weight (MW) of the proteins detecte...
<p>A. 2DE gel images of control (up) and ISO-CAs (down) with proteins of interest annotated. B. Enla...
The strategies and methods used by the QUEST system for two-dimensional gel analysis are described, ...
<p>Proteins are represented by protein type, allergen name, number of spots found and number of isoa...
<p>(A) Representative 2D-DIGE gel. Protein extracts from promastigotes of three independent biologic...
Comparing different proteomes by classical two-dimensional electrophoresis is challenging and often ...