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. 2000 Mar 21;97(7):3759–3764. doi: 10.1073/pnas.070025097

Figure 4.

Figure 4

Identification of SRK oligomeric complexes in stigma extract. (A) Proteins were extracted from stigmas expressing the S3 haplotype in a Triton X-100-containing buffer and either treated (+) or not (−) with the cross-linking reagent glutaraldehyde. Proteins then were separated by SDS/PAGE and immunoblotted with mAb 85–36-71. SRK3-containing complexes of 161 and 233 kDa are indicated by arrows. Monomeric SRK3 and eSRK3 are indicated with an asterisk and an arrowhead, respectively. (B) Velocity sedimentation on sucrose gradients. Proteins were extracted in buffer containing octyl-glucoside, and stigma extracts were either supplemented with SDS at the concentration of 0.5% (mass/vol) (+SDS) or not (−SDS). The presence of SRK3 (SRK), eSRK3 (eSRK), and SLG3 (SLG) in the different fractions was examined by immunoblotting with mAb 85–36-71 and anti-SLG3 antibodies. The distribution of molecular mass markers (66, 150, and 200 kDa) is indicated at the bottom of each panel.