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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 英文名：
HepG2
- 库存：
1x10^6/瓶
- 供应商：
上海酶研
- 肿瘤类型：
肝癌
- 细胞类型：
HepG2
- 品系：
HepG2
- 组织来源：
肝癌细胞
- 相关疾病：
详询
- 物种来源：
Human
- 免疫类型：
详询
- 细胞形态：
贴壁/悬浮
- 是否是肿瘤细胞：
是
- 器官来源：
肝癌细胞
- 运输方式：
顺丰快递
- 年限：
5年
- 生长状态：
生长良好
- 规格：
T25
HepG2、HepG2、HepG2细胞、HepG2细胞、HepG2人肝癌细胞
Cell line name Hep-G2
Synonyms HEP-G2; Hep G2; HEP G2; HepG2; HEPG2
Accession CVCL_0027
Resource Identification Initiative To cite this cell line use: Hep-G2 (RRID:CVCL_0027)
Comments Group: Patented cell line.
Problematic cell line: Misclassified. Originally thought to be a hepatocellular carcinoma cell line but shown to be from an hepatoblastoma (PubMed=19751877).
Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
Part of: ENCODE project common cell types; tier 1.
Part of: JFCR45 cancer cell line panel.
Part of: Liver Cancer Model Repository (LIMORE).
Part of: MD Anderson Cell Lines Project.
Part of: TCGA-110-CL cell line panel.
Registration: International Depositary Authority, American Type Culture Collection (ATCC); HB-8065.
Population: Caucasian.
Doubling time: 25.65 hours (PubMed=31378681); ~50-60 hours (DSMZ=ACC-180).
Omics: CTCF ChIP-seq epigenome analysis.
Omics: H3K27ac ChIP-seq epigenome analysis.
Omics: H3K27me3 ChIP-seq epigenome analysis.
Omics: H3K36me3 ChIP-seq epigenome analysis.
Omics: H3K4me1 ChIP-seq epigenome analysis.
Omics: H3K4me2 ChIP-seq epigenome analysis.
Omics: H3K4me3 ChIP-seq epigenome analysis.
Omics: H3K79me2 ChIP-seq epigenome analysis.
Omics: H3K9ac ChIP-seq epigenome analysis.
Omics: H3K9me3 ChIP-seq epigenome analysis.
Omics: H4K20me1 ChIP-seq epigenome analysis.
Omics: Deep antibody staining analysis.
Omics: Deep exome analysis.
Omics: Deep phosphoproteome analysis.
Omics: Deep proteome analysis.
Omics: Deep quantitative proteome analysis.
Omics: DNA methylation analysis.
Omics: Genome sequenced.
Omics: Metabolome analysis.
Omics: miRNA expression profiling.
Omics: Protein expression by reverse-phase protein arrays.
Omics: Secretome proteome analysis.
Omics: SNP array analysis.
Omics: Transcriptome analysis by microarray.
Omics: Transcriptome analysis by RNAseq.
Omics: Virome analysis using proteomics.
Derived from site: In situ; Liver; UBERON=UBERON_0002107.
PubMed=8224613; DOI=10.1096/fasebj.7.14.8224613
Puisieux A., Galvin K., Troalen F., Bressac B., Marcais C., Galun E., Ponchel F., Yakicier C., Ji J.-W., Ozturk M.
Retinoblastoma and p53 tumor suppressor genes in human hepatoma cell lines.
FASEB J. 7:1407-1413(1993)
PubMed=8384076; DOI=10.1016/0165-4608(93)90227-D
Chen H.-L., Chiu T.-S., Chen P.-J., Chen D.-S.
Cytogenetic studies on human liver cancer cell lines.
Cancer Genet. Cytogenet. 65:161-166(1993)
PubMed=8389256; DOI=10.1093/carcin/14.5.987
Hsu I.C., Tokiwa T., Bennett W., Metcalf R.A., Welsh J.A., Sun T., Harris C.C.
p53 gene mutation and integrated hepatitis B viral DNA sequences in human liver cancer cell lines.
Carcinogenesis 14:987-992(1993)
PubMed=7972006; DOI=10.1073/pnas.91.23.11045; PMCID=PMC45163
Okamoto A., Demetrick D.J., Spillare E.A., Hagiwara K., Hussain S.P., Bennett W.P., Forrester K., Gerwin B.I., Serrano M., Beach D.H., Harris C.C.
Mutations and altered expression of p16INK4 in human cancer.
Proc. Natl. Acad. Sci. U.S.A. 91:11045-11049(1994)
PubMed=8050184; DOI=10.1111/j.1365-2249.1994.tb06089.x; PMCID=PMC1534706
Wadee A.A., Paterson A., Coplan K.A., Reddy S.G.
HLA expression in hepatocellular carcinoma cell lines.
Clin. Exp. Immunol. 97:328-333(1994)
PubMed=8835345; DOI=10.1002/(SICI)1096-9071(199602)48:2<133::AID-JMV3>3.0.CO;2-A
Tsuboi S., Nagamori S., Miyazaki M., Mihara K., Fukaya K.-i., Teruya K., Kosaka T., Tsuji T., Namba M.
Persistence of hepatitis C virus RNA in established human hepatocellular carcinoma cell lines.
J. Med. Virol. 48:133-140(1996)
DOI=10.11418/jtca1981.16.3_173
Mihara K., Miyazaki M., Fushimi K., Tsuji T., Inoue Y., Fukaya K.-i., Ohashi R., Namba M.
The p53 gene status and other cellular characteristics of human cell lines maintained in our laboratory.
Tissue Cult. Res. Commun. 16:173-178(1997)
PubMed=9178645; DOI=10.1006/cimm.1997.1108
Nakao M., Sata M., Saitsu H., Yutani S., Kawamoto M., Kojiro M., Itoh K.
CD4+ hepatic cancer-specific cytotoxic T lymphocytes in patients with hepatocellular carcinoma.
Cell. Immunol. 177:176-181(1997)
PubMed=9359923; DOI=10.18926/AMO/30789
Mihara K., Miyazaki M., Kondo T., Fushimi K., Tsuji T., Inoue Y., Fukaya K.-i., Ishioka C., Namba M.
Yeast functional assay of the p53 gene status in human cell lines maintained in our laboratory.
Acta Med. Okayama 51:261-265(1997)
PubMed=11050057; DOI=10.1053/jhep.2000.19349
Wong N., Lai P., Pang E., Leung T.W.-T., Lau J.W.-Y., Johnson P.J.
A comprehensive karyotypic study on human hepatocellular carcinoma by spectral karyotyping.
Hepatology 32:1060-1068(2000)
PubMed=11416159; DOI=10.1073/pnas.121616198; PMCID=PMC35459
Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G., Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R., Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.
Short tandem repeat profiling provides an international reference standard for human cell lines.
Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001)
PubMed=11981770; DOI=10.1053/jhep.2002.32668
Clemens D.L., Forman A., Jerrells T.R., Sorrell M.F., Tuma D.J.
Relationship between acetaldehyde levels and cell survival in ethanol-metabolizing hepatoma cells.
Hepatology 35:1196-1204(2002)
PubMed=12029633; DOI=10.1053/jhep.2002.33683
Yasui K., Arii S., Zhao C., Imoto I., Ueda M., Nagai H., Emi M., Inazawa J.
TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomas.
Hepatology 35:1476-1484(2002)
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文献和实验*发表【中文论文】请标注：由上海酶研生物科技有限公司提供；
*发表【英文论文】请标注：From Shanghai EK-Bioscience Biotechnology Co., Ltd.
HepG2人肝肿瘤细胞株广泛应用于遗传毒理学及病毒培养等方面的研究,研究肝脏疾病发病机理及其临床应用有着重要意义。由于其与肝细胞具有相同的生物学活性，还被用于胰岛素抵抗的研究。本文对肝癌细胞培养的最佳条件做一简单综述。1、HepG2细胞的复苏条件（1）复苏温度的选择唐孟萱[1]等采用下述方法进行细胞复苏：快速将所冻存细胞40℃水浴摇床60转/ min慢摇至其溶解，溶解后马上转入 37 ℃水浴箱，手工慢摇恒温 2～3min复苏 ,复苏后 800 转/ min 离心 5min,吸去上清加入 10
HepG2人肝肿瘤细胞株广泛应用于遗传毒理学及病毒培养等方面的研究,研究肝脏疾病发病机理及其临床应用有着重要意义。由于其与肝细胞具有相同的生物学活性，还被用于胰岛素抵抗的研究。本文对肝癌细胞培养的最佳条件做一简单综述。1.HepG2细胞的复苏条件1.1 复苏温度的选择唐孟萱等采用下述方法进行细胞复苏：快速将所冻存细胞40℃水浴摇床60转/ min慢摇至其溶解，溶解后马上转入 37 ℃水浴箱，手工慢摇恒温 2～3min复苏 ,复苏后 800 转/ min 离心 5min,吸去上清加入 10
HePG2细胞属人肝肿瘤的恒生细胞株，L-02细胞则是人胎肝细胞株，二者所使用的培养基可以是一样的，即最常见的DMEM。一干使用低糖的。 细胞长满培养瓶时既要传代。使用胰酶消化即可。用D-Hank's液配制成0.25%的胰酶。使用前37度预热，细胞经PBS清洗两遍后，每个中号培养瓶加0.7ml的胰酶，胰酶的量可根据自己培养瓶的大小而定，原则就是能够盖满瓶底。加入胰酶以后，为使酶的活性最大，将培养瓶盖拧紧后放回培养箱中，3分钟左右即用含血清的培养基终止消化。如果在室温情况下消化，时间相应
技术资料