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. 2009 Nov;151(3):1546–1556. doi: 10.1104/pp.109.142729

Figure 3.

Figure 3.

Coomassie Brilliant Blue staining of proteins isolated by TAP purifications from Arabidopsis suspension cell cultures. The proteins were separated by 12% SDS-PAGE. Each gel lane was divided into a number of segments as indicated by the braces. The gel fragments were digested by trypsin overnight and subjected to LC-MS/MS for protein identification. Protein markers are as shown on the left (kD).