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    Protocol

    Detection of Glycoproteins in Gels and Blots

    As we become more aware of the significance of posttranslational modifications, such as glycosylation, in the production of recombinant proteins and in the proteomic studies of development and disease, techniq...

    Nicolle H. Packer, Malcolm S. Ball, Peter L. Devine in The Protein Protocols Handbook (2009)

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    Protocol

    Background-Free Protein Detection in Polyacrylamide Gels and on Electroblots Using Transition Metal Chelate Stains

    Electrophoretically separated proteins may be visualized using organic dyes such as Ponceau Red, Amido Black, Fast Green, or most commonly Coomassie Brilliant Blue (1,2). Alternatively, sensitive detection met...

    Wayne F. Patton in The Protein Protocols Handbook (2009)

  3. No Access

    Protocol

    Quantitative Analysis of Protein Phosphorylation Status and Protein Kinase Activity on Microarrays Using Pro-Q− Diamond Dye Technology

    The human genome is estimated to contain 30,000 to 75,000 genes, but as a result of alternative mRNA splicing and protein posttranslational modifications, the human proteome may contain a million or more prote...

    Karen Martin, Wayne F. Patton in The Proteomics Protocols Handbook (2005)

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    Protocol

    Multiplexed Proteomics Technology for the Fluorescence Detection of Phosphorylation and Protein Expression Levels Using Pro-Q® Diamond and SYPRO® Ruby Dyes

    The reversible phosphorylation of serine, threonine, and tyrosine residues is arguably one of the most important covalent posttranslational modifications regulating the functional status of proteins in eukaryo...

    Birte Schulenberg, Terrie Goodman, Thomas H. Steinberg in The Proteomics Protocols Handbook (2005)

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    Protocol

    Sensitive Quantitative Fluorescence Detection of Proteins in Gels Using SYPRO® Ruby Protein Gel Stain

    The fluorescent, noncovalent staining method, using SYPRO® Ruby dye resembles colorimetric staining procedures, such as colloidal Coomassie Blue dye staining. The dye provides noncovalent staining and is appli...

    Birte Schulenberg, Nancy Ahnert, Wayne F. Patton in The Proteomics Protocols Handbook (2005)

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    Protocol

    Rapid, Sensitive Detection of Proteins in Minigels With Fluorescent Dyes

    The advent of polyacrylamide gel electrophoresis (PAGE) in the minigel format (i.e., gel dimensions in the range of 6 × 9 cm or 8 × 8 cm × 0.75 to 1.5 mm thick), the widespread use of precast minigels, and the...

    Thomas H. Steinberg, Courtenay R. Hart in The Proteomics Protocols Handbook (2005)

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    Protocol

    Multiplexed Proteomics Technology for the Fluorescence Detection of Glycoprotein Levels and Protein Expression Levels Using Pro-Q® Emerald and SYPRO® Ruby Dyes

    Protein glycosylation is increasingly being recognized as one of the most prominent posttranslational modifications associated with malignant transformation and tumorogenesis as well as cell differentiation. T...

    Birte Schulenberg, Wayne F. Patton in The Proteomics Protocols Handbook (2005)

  8. No Access

    Protocol

    Detection of Glycoproteins in Gels and Blots

    As we become more aware of the significance of posttranslational modifications, such as glycosylation, in the production of recombinant proteins and in the proteomic studies of development and disease, techniq...

    Nicolle H. Packer, Malcolm S. Ball, Peter L. Devine in The Protein Protocols Handbook (2002)

  9. No Access

    Protocol

    Background-Free Protein Detection in Polyacrylamide Gels and on Electroblots Using Transition Metal Chelate Stains

    Electrophoretically separated proteins may be visualized using organic dyes such as Ponceau Red, Amido Black, Fast Green, or most commonly Coomassie Brilliant Blue (1,2). Alternatively, sensitive detection method...

    Wayne F. Patton in The Protein Protocols Handbook (2002)

  10. No Access

    Protocol

    Protein Detection Using Reversible Metal Chelate Stains

    Electrophoretically separated proteins may be visualized using organic dyes, such as Ponceau red, Amido black, fast green, or most commonly Coomassie Brilliant Blue (1,2). Alternatively, sensitive detection metho...

    Wayne F. Patton, Mark J. Lim, David Shepro in 2-D Proteome Analysis Protocols (1999)

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    Protocol

    Image Acquisition in 2-D Electrophoresis

    Prevalent methods for visualizing proteins resolved by two-dimensional (2-D) gel electrophoresis include autoradiography, silver staining, and Coomassie brilliant blue staining (1,2. The organic dye Coomassie bri...

    Wayne F. Patton, Mark J. Lim, David Shepro in 2-D Proteome Analysis Protocols (1999)