Results 111 to 120 of about 99,492 (163)
Some of the next articles are maybe not open access.

Two-Dimensional Difference Gel Electrophoresis

2018
Two-dimensional difference gel electrophoresis (2D DIGE) is a modified form of 2D electrophoresis (2D E) that allows one to compare two or three protein samples simultaneously on the same gel. The proteins in each sample are covalently tagged with different color fluorescent dyes that are designed to have no effect on the relative migration of proteins
Malachi, Blundon   +4 more
openaire   +2 more sources

Two-Dimensional Gel Electrophoresis Image Analysis

2021
Gel-based proteomics is still quite widespread due to its high-resolution power; the experimental approach is based on differential analysis, where groups of samples (e.g., control vs diseased) are compared to identify panels of potential biomarkers.
Robotti E., Cala Elisa, Marengo E.
openaire   +3 more sources

Alignment of two-dimensional electrophoresis gels

Biochemical and Biophysical Research Communications, 2007
Two-dimensional electrophoresis is a major separating technique for proteins in proteomics. Alignment of gel images is critical for intra-laboratory or even more difficult inter-laboratory gel comparisons. In the paper, we propose a novel iterative closest point (ICP) method for 2D-gel electrophoresis image alignment.
Shi, Guihua   +4 more
openaire   +3 more sources

Two-Dimensional Difference Gel Electrophoresis

2012
Two-dimensional difference gel electrophoresis (2D DIGE) is a modified form of 2D electrophoresis (2DE) that allows one to compare two or three protein samples simultaneously on the same gel. The proteins in each sample are covalently tagged with different color fluorescent dyes that are designed to have no effect on the relative migration of proteins ...
openaire   +2 more sources

Dialysis‐assisted two‐dimensional gel electrophoresis

ELECTROPHORESIS, 2006
Abstract2‐DE is an important tool in proteomics research. However, intrinsic gel‐to‐gel variability of 2‐DE often masks the biological differences between the samples and compromises quantitative comparison of protein expression levels. Here, we describe a modification of 2‐DE that results in improved matching and quantification of proteins.
Olivier, Danos, Fedor, Svinartchouk
openaire   +2 more sources

Two-Dimensional Difference Gel Electrophoresis

2009
The introduction of two-dimensional fluorescent difference gel electrophoresis has enabled the extensive screening of differential protein expression levels with higher confidence and greater sensitivity than using the classical two-dimensional electrophoresis (2DE) approach.
openaire   +2 more sources

Two-dimensional gel electrophoresis of proteins

Journal of Chromatography B: Biomedical Sciences and Applications, 1987
The high-resolution capacity of two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) makes it an excellent tool for the analysis and characterisation of complex protein mixtures. The evolution of two-dimensional electrophoresis is briefly described.
openaire   +2 more sources

High Resolution Two-dimensional Polyacrylamide-gel Electrophoresis

TrAC Trends in Analytical Chemistry, 1983
Abstract The combination of two different gel electrophoretic techniques in a two-dimensional separation procedure provides the resolution capacity required for the simultaneous separation and analysis of complex protein mixtures. This technique is therefore a powerful tool for the study of phenotypic expression.
Michael J. Dunn, Arthur H.M. Burghes
openaire   +1 more source

Two‐Dimensional Blue Native Polyacrylamide Gel Electrophoresis

Current Protocols in Cell Biology, 2008
AbstractMultiprotein complexes play crucial roles in nearly all cell biological processes. Blue Native Polyacrylamide Gel Electrophoresis (BN‐PAGE) is a powerful method to study these complexes. It is a native protein separation method that relies on the dye Coomassie blue to confer negative charge for separation.
openaire   +3 more sources

Two-dimensional agarose gel electrophoresis without gel manipulation

Analytical Biochemistry, 1985
The apparatus and procedure to perform two-dimensional agarose gel electrophoresis without manipulating the gel used for the first electrophoresis (first-dimension gel) have been developed. The procedure is less complex, less damaging to first-dimension gels, and more precise than procedures that require manipulation of the first-dimension gel.
openaire   +2 more sources

Home - About - Disclaimer - Privacy