A comparison between Sypro Ruby and ruthenium II tris (bathophenanthroline disulfonate) as fluorescent stains for protein detection in gels A comparison between two fluorescent metal chelates for staining proteins separated by electrophoresis has been carried out. One of these chelates is ruthenium II tris (bathophenanthroline disulfonate) and the other is commercial Sypro Ruby. Both can be efficiently detected either with UV tables or with commercial laser fluorescence scanners. The sensitivity and homogeneity of the stains and the interference with mass spectrometry analysis have been investigated. It appears that both stains per-form similarly for protein detection, while ruthenium II tris (bathophenanthroline disul-fonate) performs bett...
The author presents a novel rapid, low-cost staining protocol (hot water protocol) for proteins in a...
Lightning Fast is a sensitive fluorescence-based stain for detecting proteins in onedimensional and ...
International audienceProtein detection on SDS gels or on 2-D gels must combine several features, su...
Silver staining has been the method most commonly employed for high sensitivity staining of proteins...
A statistical comparison of silver and SYPRO Ruby staining for proteomic analysis Silver staining ha...
The in-gel detection of proteins for various proteomic experiments is commonly done with the fluores...
<p>This article reports a new class of luminescent metal complexes, biscyclometalated iridium(III) c...
This paper describes the use of a ruthenium complex ((bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyri...
Gel electrophoresis, particularly one-dimensional electrophoresis (1DE) and two-dimensional electrop...
With the recent introduction of new fluorescence stains to the proteomics market, there is now more ...
Staining techniques are the primary method for quantitative detection of gel-resolved proteins. With...
International audienceSilver staining is used to detect proteins after electrophoretic separation on...
Proteomics research relies heavily on visualization methods for detection of proteins separated by p...
Proteins are a distinct class of biological molecules involved in all cellular processes. The protei...
Staining of two-dimensional gels is a primary concern in proteomic studies using two-dimensional gel...
The author presents a novel rapid, low-cost staining protocol (hot water protocol) for proteins in a...
Lightning Fast is a sensitive fluorescence-based stain for detecting proteins in onedimensional and ...
International audienceProtein detection on SDS gels or on 2-D gels must combine several features, su...
Silver staining has been the method most commonly employed for high sensitivity staining of proteins...
A statistical comparison of silver and SYPRO Ruby staining for proteomic analysis Silver staining ha...
The in-gel detection of proteins for various proteomic experiments is commonly done with the fluores...
<p>This article reports a new class of luminescent metal complexes, biscyclometalated iridium(III) c...
This paper describes the use of a ruthenium complex ((bis(2,2'-bipyridine)-4'-methyl-4-carboxybipyri...
Gel electrophoresis, particularly one-dimensional electrophoresis (1DE) and two-dimensional electrop...
With the recent introduction of new fluorescence stains to the proteomics market, there is now more ...
Staining techniques are the primary method for quantitative detection of gel-resolved proteins. With...
International audienceSilver staining is used to detect proteins after electrophoretic separation on...
Proteomics research relies heavily on visualization methods for detection of proteins separated by p...
Proteins are a distinct class of biological molecules involved in all cellular processes. The protei...
Staining of two-dimensional gels is a primary concern in proteomic studies using two-dimensional gel...
The author presents a novel rapid, low-cost staining protocol (hot water protocol) for proteins in a...
Lightning Fast is a sensitive fluorescence-based stain for detecting proteins in onedimensional and ...
International audienceProtein detection on SDS gels or on 2-D gels must combine several features, su...