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PCR and sequencing revealed that hIL-24 gene was successfully cloned into plasmid pcDNA3.1(+) and its eukaryotic expression vector was constructed. The vector was able to express hIL-24 protein after transfected into Ca Ski cells.
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PCR及测序结果均证实成功克隆了人IL-24基因;构建了真核表达质粒pcDNA3.;1(+)-hIL-24;该质粒被转染入Ca Ski细胞中能表达出hIL-24蛋白
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