Figure 1.

Western blot and protein quantification for WT and T5 SBPase transformants. Blots were probed using antibodies raised against SBPase and transketolase. Proteins were detected using horseradish peroxidase conjugated to the secondary antibody. Gels were loaded on an equal protein basis. a) Upper blot is SBPase and the lower is Transketolase (TK) as a loading control. Each lane is a separate individual. b) Quantification for SBPase and TK is based on n = 6 transformants vs. n = 5 WT in ambient CO₂.