Detection of proteins in sodium dodecyl sulfate-polyacryl-amide gel electrophoresis (SDS-PAGE) is an important first step for protein analysis. For years, various experimental efforts have been directed to develop and improve the protein detection methods1-4 with particular interests in their sensitivity. Among the available protein detection methods, staining with Coomasie brilliant blue (CBB) is most frequently used in laboratories. However, despite the popularity of the method, its sensitivity is still low, and needs to be improved significantly for detecting low-abundance proteins in analytical 2-D gels for proteomic applications. Previously, Neuhoff et al. successfully increased the sensitivity of CBB staining by using large amount of ...
Modified colloidal Coomassie Brilliant Blue (cCBB) staining utilising a novel destain protocol and n...
Native polyacrylamide gel electrophoresis (PAGE) and sodium dodecyl sulfate (SDS)–PAGE are among the...
Also published as a book chapter: Proteomics, 2009 / J. Reinders and A. Sickmann (eds.), Ch.4 pp.59-...
Gel electrophoresis, particularly one- (1DE) and two-dimensional electrophoresis (2DE), remain among...
Gel electrophoresis, particularly one-dimensional electrophoresis (1DE) and two-dimensional electrop...
Staining techniques are the primary method for quantitative detection of gel-resolved proteins. With...
The time required to visualize proteins using Coomassie Blue dye has been significantly reduced with...
The time required to visualize proteins using Coomassie Blue dye has been significantly reduced with...
Proteomics research relies heavily on visualization methods for detection of proteins separated by p...
Modified colloidal Coomassie Brilliant Blue (cCBB) staining utilising a novel destain protocol and n...
Coomassie brilliant blue (CBB) dyes have been commonly used for the staining of protein bands in pol...
Proteins are a distinct class of biological molecules involved in all cellular processes. The protei...
Procedures in life sciences research laboratories often require chemicals and plasticware that are c...
International audienceSilver staining is used to detect proteins after electrophoretic separation on...
Quantitative comparative proteomics require accurate and reproducible assessments of total protein c...
Modified colloidal Coomassie Brilliant Blue (cCBB) staining utilising a novel destain protocol and n...
Native polyacrylamide gel electrophoresis (PAGE) and sodium dodecyl sulfate (SDS)–PAGE are among the...
Also published as a book chapter: Proteomics, 2009 / J. Reinders and A. Sickmann (eds.), Ch.4 pp.59-...
Gel electrophoresis, particularly one- (1DE) and two-dimensional electrophoresis (2DE), remain among...
Gel electrophoresis, particularly one-dimensional electrophoresis (1DE) and two-dimensional electrop...
Staining techniques are the primary method for quantitative detection of gel-resolved proteins. With...
The time required to visualize proteins using Coomassie Blue dye has been significantly reduced with...
The time required to visualize proteins using Coomassie Blue dye has been significantly reduced with...
Proteomics research relies heavily on visualization methods for detection of proteins separated by p...
Modified colloidal Coomassie Brilliant Blue (cCBB) staining utilising a novel destain protocol and n...
Coomassie brilliant blue (CBB) dyes have been commonly used for the staining of protein bands in pol...
Proteins are a distinct class of biological molecules involved in all cellular processes. The protei...
Procedures in life sciences research laboratories often require chemicals and plasticware that are c...
International audienceSilver staining is used to detect proteins after electrophoretic separation on...
Quantitative comparative proteomics require accurate and reproducible assessments of total protein c...
Modified colloidal Coomassie Brilliant Blue (cCBB) staining utilising a novel destain protocol and n...
Native polyacrylamide gel electrophoresis (PAGE) and sodium dodecyl sulfate (SDS)–PAGE are among the...
Also published as a book chapter: Proteomics, 2009 / J. Reinders and A. Sickmann (eds.), Ch.4 pp.59-...