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. Author manuscript; available in PMC: 2010 Jul 29.
Published in final edited form as: J Proteome Res. 2008 Sep 4;7(10):4603–4608. doi: 10.1021/pr800456q

Figure 3.

Figure 3

An in vitro-modified peptide with a mass shift of +108 at cysteine. BSA (300 ng) was resolved by SDS-PAGE and stained with colloidal Coomassie staining solution composed of 9 vol of G−250 stain solution (ProtoBlue, National Diagnostics, Atlanta, GA) and 1 vol of ethanol. The gel band was destained with buffer composed of ethanol/water (50:50, v/v) before in-gel digestion and HPLC/MS/MS analysis.