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1)  HepG2
人肝癌细胞株
1.
Objective To investigate the effect of Acanthopanax senticosus saponin (ASS)on the protein and mRNA expression of vascular endothelial growth factor (VEGF) in human HepG2.
方法以人肝癌细胞株(HepG2)为研究对象,分别用ELISA及RT-PCR检测ASS对HepG2细胞VEGF蛋白及mRNA水平表达的影响。
2.
Aim:To study the effect of abnormal savda Munziq ethyl acetate extract(ASMq-EtOAc) on the proliferation,apoptosis and correlative gene expression in human hepatoma(HepG2) cells in order to elucidate the molecular mechanisms for the anticancer activity of abnormal savda Munziq.
目的:观察异常黑胆质成熟剂乙酸乙酯萃取物(ASMq-EtOAc)对人肝癌细胞株(HepG2)生长和凋亡及相关基因调控的作用,探讨其抗癌的物质基础和作用机理。
3.
Objective To observe the DNA strand breaks in HepG2 cell induced by styrene and to evaluate the antagonistic effect of natural cow-bezoar and bilirubin on DNA strand breaks induced by styrene.
目的 观察苯乙烯诱导的人肝癌细胞株 (HepG2 )细胞DNA链断裂损伤以及天然牛黄和胆红素对其损伤的拮抗效应。
2)  Human hepatoma cell line
人肝癌细胞株
3)  Human hepatoma carcinoma cell
人肝癌细胞株
1.
METHODS:Human hepatoma carcinoma cell lines HepG2 2,2,15,which were transfected from HBV DNA,were taken as target cells,cells were cultured with different concentrations of test drugs, with HBsAg,HBeAg and HBV DNA in the cultured supernatant determined by time-resolved immunofluorometric assay and fluorescent quantitation PCR assay on day 6th and 10th day,meanwhile,with.
方法:以HBVDNA转染的人肝癌细胞株HepG22,2,15细胞为靶细胞,以不同浓度的试验药物培养细胞,在第6天、第10天时应用时间分辨免疫荧光分析法和荧光实时定量聚合酶链反应法检测培养基上清液中HBsAg、HBeAg和HBVDNA,同时应用MTT法检测药物对细胞的毒性。
4)  HepG2 cell lines
人肝癌细胞株HepG2
5)  Human hepatocarcinoma cell line QSG-7701
人肝癌7701细胞株
6)  human HepG2 cell line
人肝癌HepG2细胞株
1.
In this thesis, its antitumor mechanism was studied with human HepG2 cell line as the test material through MTT, AO/EB double staining and RT-PCR.
本论文以人肝癌HepG2细胞株为试验材料,分别应用MTT比色法、AO/EB双染色法、RT-PCR技术,研究隐丹参酮对癌症的抑制作用机制,获得了如下结果: 1)通过不同浓度的隐丹参酮刺激人肝癌HepG2细胞株6,12,18,24小时后分别用MTT比色法检测其OD值。
补充资料:细胞株
分子式:
CAS号:

性质:用单细胞分离培养法或克隆形成法从原代培养或从细胞系所选出的细胞群,称细胞株。一个细胞株应具有特定的生物学性质和标记并持续存在。

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