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A few plasmids (pGL1124, pGL1224 and pGL1217) had been manufactured to enable the replacement of one allele of CYC9To research the subcellular localization on the CRK12 protein, a pEarleyGate104 vector was employed for a transient expression with the CRK12 protein fused to yellow fluorescent protein (YFP). The confocal images with the P. vulgarisge