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Construction and expression of recombined human AFP eukaryotic expression vector

机译:重组人AFP真核表达载体的构建及表达

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摘要

AIM: To construct a recombined human AFP eukaryotic expression vector for the purpose of gene therapy and target therapy of hepatocellular carcinoma (HCC).METHODS: The full length AFP-cDNA of prokaryotic vector was digested, and subcloned to the multi-clony sites of the eukaryotic vector. The constructed vector was confirmed by enzymes digestion and electrophoresis, and the product expressed was detected by electrochemiluminescence and immunofluorescence methods.RESULTS: The full length AFP-cDNA successfully cloned to the eukaryotic vector through electrophoresis, 0.9723 IU/mL AFP antigen was detected in the supernatant of AFP-CHO by electrochemiluminescence method. Compared with the control groups, the differences were significant (P < 0.05). AFP antigen molecule was observed in the plasma of AFP-CHO by immunofluorescence staining.CONCLUSION: The recombined human AFP eukaryotic expression vector can express in CHO cell line. It provides experimental data for gene therapy and target therapy of hepatocellular carcinoma.
机译:目的:构建重组人AFP真核表达载体,用于肝细胞癌(HCC)的基因治疗和靶向治疗。方法:消化原核载体全长AFP-cDNA,并亚克隆至人肝癌的多克隆位点。真核载体。结果:经电泳成功克隆出全长AFP-cDNA,真核表达载体检测到0.9723 IU / mL的AFP抗原,经酶切和电泳鉴定,表达的产物通过电化学发光和免疫荧光法检测。电化学发光法测定AFP-CHO的上清液。与对照组相比,差异有统计学意义(P <0.05)。结论:重组人AFP真核表达载体可在CHO细胞中表达,可在AFP-CHO血浆中观察到AFP抗原分子。它为肝细胞癌的基因治疗和靶向治疗提供实验数据。

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