AbstractProteomics requires an optimized level of sample-processing, including a minimal sample-processing time and an optimal peptide recovery from protein digests, in order to maximize the percentage sequence coverage and to improve the accuracy of protein identification. The conventional methods of protein characterization from one-dimensional or two-dimensional gels include the destaining of an excised gel piece, followed by an overnight in-gel enzyme digestion. The aims of this study were to determine whether: (1) stained gels can be used without any destaining for trypsin digestion and mass spectrometry (MS); (2) tryptic peptides can be recovered from a matrix-assisted laser desorption/ionization (MALDI) target plate for a subsequent ...
A methodology has been developed for the rapid identification of gel separated proteins. Following i...
Pre-fractionation by gel electrophoresis is often combined with liquid chromatography-mass spectrome...
The combination of gel-based two-dimensional protein separations with protein identification by matr...
Sample preparation is crucial to the success of experiments in biological mass spectrometry. In prot...
Proteins with molecular mass ( M r ) <20 kDa are often poorly separated in 2-D sodium dodecyl sulfa...
The in‐gel digestion of proteins for analysis by liquid chromatograph mass spectrometry has been use...
AbstractA comparative analysis of protein identification for a total of 162 protein spots separated ...
Despite tremendous advances in mass spectrometry instrumentation and mass spectrometry-based methodo...
We tested a semiautomated protocol for the proper storage and conservation in a hospital biobank of ...
We tested a semiautomated protocol for the proper storage and conservation in a hospital biobank of ...
Protein spots from two-dimensional (2-D) gel electrophoresis of a human erythroleukemia cell line ha...
Proteins are the workhorses of biology, playing multifaceted roles in maintaining cellular function,...
Peptide generation by trypsin digestion is typically the first step in mass spectrometry-based prote...
Proteome studies aim to link gene to function. Instead of screening for function in a specific prote...
The combination of gel-based two-dimensional protein separations with protein identification by matr...
A methodology has been developed for the rapid identification of gel separated proteins. Following i...
Pre-fractionation by gel electrophoresis is often combined with liquid chromatography-mass spectrome...
The combination of gel-based two-dimensional protein separations with protein identification by matr...
Sample preparation is crucial to the success of experiments in biological mass spectrometry. In prot...
Proteins with molecular mass ( M r ) <20 kDa are often poorly separated in 2-D sodium dodecyl sulfa...
The in‐gel digestion of proteins for analysis by liquid chromatograph mass spectrometry has been use...
AbstractA comparative analysis of protein identification for a total of 162 protein spots separated ...
Despite tremendous advances in mass spectrometry instrumentation and mass spectrometry-based methodo...
We tested a semiautomated protocol for the proper storage and conservation in a hospital biobank of ...
We tested a semiautomated protocol for the proper storage and conservation in a hospital biobank of ...
Protein spots from two-dimensional (2-D) gel electrophoresis of a human erythroleukemia cell line ha...
Proteins are the workhorses of biology, playing multifaceted roles in maintaining cellular function,...
Peptide generation by trypsin digestion is typically the first step in mass spectrometry-based prote...
Proteome studies aim to link gene to function. Instead of screening for function in a specific prote...
The combination of gel-based two-dimensional protein separations with protein identification by matr...
A methodology has been developed for the rapid identification of gel separated proteins. Following i...
Pre-fractionation by gel electrophoresis is often combined with liquid chromatography-mass spectrome...
The combination of gel-based two-dimensional protein separations with protein identification by matr...