人肝癌细胞株,HepG2
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。
英文短句/例句

1.The Expression of STAT 5 in human hepatocellular carcinoma cell line SMMC-7721STAT5在人肝癌细胞株SMMC-7721细胞内的表达
2.Expression of VEGF/VEGFR in Human Hepatoma Cell Lines and Its Role in the Growth of the Cells in Vivo;人肝癌细胞株VEGF/VEGFR表达及成瘤性研究
3.The Experimental Study of the Effect of Hyperthermia on the Apoptosis of Human Hepatoma Cell Line Hep-G2热疗对人肝癌细胞株Hep-G2细胞凋亡的实验研究
4.Effects of GHSC-73 on proliferation and cell cycle of human hepatocellular carcinoma HepG2 cellsGHSC-73对人肝癌细胞株HepG2细胞增殖及细胞周期的影响
5.Effects of sFRP2 on Biological Behaviors of Human Hepatoma Cell Line HepG2;sFRP2对人肝癌细胞株HepG2生物学行为的影响
6.Enhancing Radiosensitivity of Oxaliplatin on Human Hepatoma Cell Lines SMMC-7721;奥沙利铂对人肝癌细胞株SMMC-7721放射增敏作用
7.Effect of Tea Polyphenols on Cell Cycle of Human Liver Cancer Cell;茶多酚对人肝癌细胞株SMMC-7721的生物效应
8.Inhibiting Telomerase Activity of Liver Cancer Cell Line SMMC-7721 by Antisense hTRT;反义hTRT对人肝癌细胞株SMMC-7721端粒酶的抑制作用
9.Study of shRNA Silencing Kir6.2 Gene in SK-Hep1 Cell Strains of Human Hepatocellular Carcinoma;shRNA沉默人肝癌细胞株SK-Hep1 Kir6.2基因的研究
10.Experimental study on the therapeutic effectiveness of combined use of allicin with ADM on human hepatocarcinoma cancer QGY-7701 cells大蒜素联合阿霉素诱导人肝癌细胞株QGY-7701凋亡
11.EFFECTS OF THALIDOMIDE ON PROLIFERATION OF HUMAN HEPATOMA SMMC-7721 CELLS IN VITRO沙利度胺对人肝癌细胞株SMMC-7721体外增殖影响
12.DEPRESSANT EFFECTS OF SORAFENIB ON HUMAN LIVER CANCER CELL LINE HEPG2索拉菲尼对人肝癌细胞株HepG2抑制作用的研究
13.Antitumor Effects of Oxaliplatin on Human Hepatocellular Carcinoma SMMC7721 Cells in vitro奥沙利铂对人肝癌细胞株SMMC7721的体外抗肿瘤作用
14.EFFECTS OF HYPERTHERMIA ON GROWTH OF HEPATOMA CELL LINE HEPG2 IN VITRO热疗对人肝癌细胞株HepG2生长影响的体外研究
15.Effects of MT1-MMP on biological behavour of human hepatocellular carcinoma cells HepG2MT1-MMP对人肝癌细胞株HepG2生物学行为的影响
16.Detection of iASPP mRNA in Hepatocellular Carcinoma and Hepatoma Cell Lines by Fluorescence Quantitative RT-PCR.;实时荧光定量RT-PCR检测肝癌及人肝癌细胞株iASPP mRNA
17.Expressions of NAP-2 protein in human hepatoma cell line SMCC-7721 and hepatocellular carcinoma tissues嗜中性活性肽2(NAP-2)在人肝癌细胞株和肝癌组织的表达
18.Influnce of curcumin on the apoptosis and cell cycle distribution of HepG2 cells姜黄素对人肝癌细胞株HepG2凋亡和细胞周期的影响
相关短句/例句

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。
延伸阅读

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。