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BTPR_1513_sm_SuppFig1.doc128KFigure S-1. Schematic illustration of cphA gene into an expression vector pET-21b by a modified restriction-free cloning method. The cphA gene of Synechocystis sp. PCC 6803 was cloned into pET-21b(+) vector by a modified restriction-free cloning method. After three stages of PCR, the parental pET-21b(+) vector was degraded by DpnI, and the remaining products were transformed to competent E. coli.

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