慢病毒
重组DNA
克隆(Java方法)
RNA干扰
细胞培养
转染
分子生物学
生物
基因
效价
结直肠癌
病毒学
小发夹RNA
载体(分子生物学)
病毒载体
癌症研究
核糖核酸
癌症
病毒
遗传学
病毒性疾病
作者
Juan Yao,Yan-qing Ding,Jun Zhou,Yuhong Liu,Jian‐Ming Li
出处
期刊:PubMed
日期:2009-04-01
卷期号:29 (4): 593-7
摘要
To establish a colorectal cancer cell line with stable PRL-3 and CDH22 gene knock-down for investigating the role of PRL-3 and CDH22 genes in the carcinogenesis and metastasis of colorectal cancer.A recombinant lentiviral vector targeting CDH22 gene was obtained using the pENTRTM/U6 construct and pLenti6/BLOCK-iT (TM)-DEST vector. The recombinant lentivirus was harvested from 293FT cells cotransfected with the optimized ViraPower(TM) Packaging Mix and the pLenti6/BLOCK-iT(TM)-DEST expression construct. SW480/PRL-3- cells were infected with the recombinant lentivirus targeting CDH22, and SW480 cells with stable PRL-3 and CDH22 knock-down were screened by blasticidin selection. PRL-3 expression in the cells was determined by real-time RT-PCR. RESULTS The titer of the lentivirus for the second infection was 8 x 10(5) U/ml. Seventeen positive clones were selected, among which the Clone 1 exhibited substantially down-regulated CDH22 and PRL-3 mRNA expressions.A human colorectal cancer cell line with stable PRL-3 and CDH22 gene knock-down has been established.
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