Objective to investigate the gene transduction efficiency of lentiviral vector in leukemia cells to provide key basis for leukemia gene therapy.
目的：探讨慢病毒载体在白血病细胞中的基因转导效率，为白血病基因治疗提供关键依据。
Objective: To study the inhibition of OPCML to ovarian cancer cell lines using a lentiviral vector system for efficient gene transduction.
目的：探讨重组慢病毒介导的体外转导OPCML基因的可行性及其对卯巢上皮性癌（卵巢癌）细胞的抑制作用。
Abstract: Objective to investigate the gene transduction efficiency of lentiviral vector in leukemia cells to provide key basis for leukemia gene therapy.
目的：探讨慢病毒载体在白血病细胞中的基因转导效率，为白血病基因治疗提供关键依据。
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