To investigate the function of PRAK in vivo, a GST fusion protein of PRAK was used as a bait and screened through T7 phage display system.
为了研究PRAK在细胞内的确切功能，我们利用GST-PRAK作为诱饵，通过T7噬菌体展示系统进行了筛选。
Using the PDZ domain in LNX protein as bait, we screened for LNX-interacting proteins by yeast-2-hybrid system.
采用酵母双杂交系统，我们用LNX蛋白中的PD Z结构域为诱饵，筛选相互作用蛋白。
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