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For Co-IP, cell lysate was prepared for WB assay, and 1.01.2 mg proteins were incubated with normal rabbit IgG (as control) for 2 h, and followed by 2 h incubation with 20 L protein A/G-beads

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The measured velocities were corrected by subtracting the rate of spontaneous non-enzymatic reaction and three independent experiments were performed at each substrate concentration

A Phytochrome B-PIF4-MYC2/MYC4 module inhibits secondary cell wall thickening in response to shaded light

Quantitative characterization of the influence of the nanoscale morphology of nanostructured surfaces on bacterial adhesion and biofilm formation