1986ACTA HISTOCHEMICA ET CYTOCHEMICAOpen access

NEGATIVE GOLD STAINING FOR ELECTROPHORETIC PROTEIN PROFILE INTERPRETATIONS

Bruce Budowle, Anne M. Gambel

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Abstract

A simple method was described for negative gold staining of ultrathin-layer polyacrylamide gels. The protein bands were clear (unstained) and sharp while the gel matrix was pink-purple. Negative gold staining was up to five-fold more sensitive than coomassie blue, but an order of magnitude less sensitive than silver staining for protein detection. However, there were examples where negative gold staining was able to detect particular proteins not effectively stained by coomassie blue or silver.

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A simple method was described for negative gold staining of ultrathin-layer polyacrylamide gels. The protein bands were clear (unstained) and sharp while the gel matrix was pink-purple. Negative gold staining was up to five-fold more sensitive than coomassie blue, but an order of magnitude less sensitive than silver staining for protein detection. However, there were examples where negative gold staining was able to detect particular proteins not effectively stained by coomassie blue or silver.

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Available abstract

A simple method was described for negative gold staining of ultrathin-layer polyacrylamide gels. The protein bands were clear (unstained) and sharp while the gel matrix was pink-purple. Negative gold staining was up to five-fold more sensitive than coomassie blue, but an order of magnitude less sensitive than silver staining for protein detection. However, there were examples where negative gold staining was able to detect particular proteins not effectively stained by coomassie blue or silver.

Key concepts: Staining, Silver stain, Coomassie Brilliant Blue, Chemistry, Electrophoresis, Protein detection, Negative stain, Polyacrylamide gel electrophoresis

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