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. Author manuscript; available in PMC: 2015 May 1.
Published in final edited form as: Plant J. 2014 Apr 15;78(3):491–515. doi: 10.1111/tpj.12490

Figure 1.

Figure 1

Simplified diagram showing complementary approaches of saturation DIGE and ICAT used to identify redox sensitive proteins. Proteins from control and hormone-treated guard cells were first alkylated to block remaining free -SH groups, then the cysteines oxidized were reduced and labeled with Cy dyes or ICAT reagents, followed by DIGE and LC-MS/MS. IAM, iodoacetamide; CAM, carbamidomethylation; TCEP, tris(2-carboxyethyl)phosphine.