Human HepG2 Hepatocellular Carcinoma Cells

Cellular Engineering Technologies

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CET-CR1015-500
  • Human HepG2 Hepatocellular Carcinoma Cells
  • Human HepG2 Hepatocellular Carcinoma Cells
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HepG2 Hepatocellular Carcinoma Cells

HepG2 Hepatocellular Caincoma Cells are a widely used human hepatocellular carcinoma (HCC) cell line derived from a liver biopsy of a 14-year-old male donor. These cells serve as a critical model system for studying liver function, cancer biology, drug metabolism, and hepatotoxicity [i]. With their ability to produce major plasma proteins, HepG2 cells provide a robust platform for analyzing liver-specific processes, including metabolism, protein secretion, and tumor progression.

HepG2 cells are commonly used to investigate various aspects of liver disease, including carcinogenesis, tumor metastasis, and cytotoxic responses to drugs and environmental toxins. Moreover, these cells secrete essential plasma proteins such as albumin, α2-macroglobulin, α1-anti-trypsin, and plasminogen, making them ideal for protein-based assays, molecular biology applications, and biochemical studies. As a result, their versatility enables research into key hepatic functions, including lipid metabolism, glucose regulation, and drug detoxification.

As an immortalized hepatic cell line, HepG2 cells offer a homogeneous and reproducible alternative to primary hepatocytes, eliminating the need for liver biopsies. They exhibit a characteristic growth pattern, initially proliferating slowly and forming clusters rather than a traditional monolayer. Their adaptability and well-documented behavior make them an invaluable resource for studying liver disease mechanisms, pharmaceutical development, and toxicology assessments.

Product Specifications

  • Source: Liver biopsy from a 14-year-old male donor
  • Cell Type: Human hepatocellular carcinoma cell line
  • Secretion Profile: Albumin, α2-macroglobulin, α1-anti-trypsin, plasminogen
  • Applications:
    • Cancer research and drug discovery
    • Liver metabolism and toxicology studies
    • Signaling pathway analysis
    • Protein expression and molecular biology research
    • Spheroid genotoxicity testing [ii]
  • Growth Characteristics: Cluster-forming with slow initial proliferation

Recommended Products for HepG2 Cells

  • HepG2 Hepatocellular Carcinoma Expansion Media (CET-MR1010)
  • Human HepG2 Research Starter Kit (CET-BR1003)

Shipping & Storage

  • Vial Size: Approximately 500,000 cells
  • Shipping Conditions: Shipped on dry ice to maintain viability
  • Storage Recommendation: Store in liquid nitrogen vapor phase for long-term preservation

HepG2 cells continue to be a cornerstone in liver disease research, offering a reliable and well-characterized model for studying hepatocellular carcinoma, drug metabolism, and liver toxicity. Their ability to produce key liver proteins and respond to environmental and pharmaceutical agents makes them indispensable for academic and commercial research.





Documents & Links for Human HepG2 Hepatocellular Carcinoma Cells
Datasheet Human HepG2 Hepatocellular Carcinoma Cells Datasheet
Vendor Page Human HepG2 Hepatocellular Carcinoma Cells at Cellular Engineering Technologies

Documents & Links for Human HepG2 Hepatocellular Carcinoma Cells
Datasheet Human HepG2 Hepatocellular Carcinoma Cells Datasheet
Vendor Page Human HepG2 Hepatocellular Carcinoma Cells



Citations for Human HepG2 Hepatocellular Carcinoma Cells – 20 Found
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Asai, Akira; Yasuoka, Hidetaka; Matsui, Masahiro; Tsuchimoto, Yusuke; Fukunishi, Shinya; Higuchi, Kazuhide. Programmed Death 1 Ligand Expression in the Monocytes of Patients with Hepatocellular Carcinoma Depends on Tumor Progression. Cancers. 2020;12(8)  PubMed
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Udagawa, Daisuke; Nagata, Shogo; Yagi, Hiroshi; Nishi, Kotaro; Morisaku, Toshinori; Adachi, Shungo; Nakano, Yutaka; Tanaka, Masayuki; Hori, Shutaro; Hasegawa, Yasushi; Abe, Yuta; Kitago, Minoru; Kitagawa, Yuko. A Novel Approach to Orthotopic Hepatocyte Transplantation Engineered With Liver Hydrogel for Fibrotic Livers, Enhancing Cell-Cell Interaction and Angiogenesis. Cell Transplantation. 2024;33:9636897241253700.  PubMed
Minami, Tatsuro; Satoh, Kimio; Nogi, Masamichi; Kudo, Shun; Miyata, Satoshi; Tanaka, Shin-ichi; Shimokawa, Hiroaki. Statins up-regulate SmgGDS through β1-integrin/Akt1 pathway in endothelial cells. Cardiovascular Research. 2016;109(1):151-61.  PubMed
Yasuoka, Hidetaka; Asai, Akira; Ohama, Hideko; Tsuchimoto, Yusuke; Fukunishi, Shinya; Higuchi, Kazuhide. Increased both PD-L1 and PD-L2 expressions on monocytes of patients with hepatocellular carcinoma was associated with a poor prognosis. Scientific Reports. 2020;10(1):10377.  PubMed
Tani, Naoto; Ikeda, Tomoya; Ishikawa, Takaki. Relationship between clock gene expression and CYP2C19 and CYP3A4 with benzodiazepines. Human & Experimental Toxicology. 2023;42:9603271231171643.  PubMed
Tani, Naoto; Ikeda, Tomoya; Ishikawa, Takaki. Effect of methamphetamine on clock genes and drug-metabolizing enzyme expression. Human & Experimental Toxicology. 2022;41:9603271221124092.  PubMed