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Hepa 1-6
Tissue
肝脏
Disease
肝细胞癌
Synonyms
HEPA 1-6, Hepa-1-6, Hepa1-6

Documents

Hepa 1-6

Cell line · Product number 400474

The Hepa 1-6 cell line is a well-characterized model derived from a hepatoma induced in an adult mouse. This cell line is commonly used in biomedical rese...

US$395.00excl. tax and shipping
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Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

Hepa 1-6 细胞系是一种从成年小鼠诱发的肝癌中提取的特征良好的模型。这种细胞系常用于生物医学研究,重点研究肝癌、肝脏代谢和毒理学。细胞呈上皮形态,表现出未分化肝细胞癌的表型。Hepa 1-6 对研究肝功能中的生化途径和肝癌发生的细胞机制尤为重要。

肝 1-6 细胞易于培养,并能在标准实验室条件下保持稳定的生长和繁殖。它们能表达多种细胞色素 P450 酶,是药理学和毒理学研究的绝佳工具。这些细胞还可用于探索肝细胞中基因表达的调控,了解各种物质对肝功能的影响。由于 Hepa 1-6 生长旺盛且与人类肝脏疾病密切相关,因此仍是肝脏疾病研究领域的重要资源。

Tissue
肝脏
Disease
肝细胞癌
Synonyms
  • HEPA 1-6
  • Hepa-1-6
  • Hepa1-6

02Classification

Organism
Mouse
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮样
Tumourigenic
是的,在 C57BL/6 小鼠中。
Doubling time
25 小时

04Identifiers

Citation
Hepa 1-6(Cytion 目录编号 400474)
NCBI TaxID
10090
Cellosaurus
CVCL_0327

05Expression and susceptibility

Viruses
外胚叶病毒(鼠痘):阴性
Products
白蛋白、甲胎蛋白(AFP,甲胎蛋白)、白蛋白、甲型抗胰蛋白酶(甲型-1-抗胰蛋白酶)、淀粉酶

06Handling and culture

Culture medium
DMEM:Ham's F12(1:1),w: 3.1 g/L 葡萄糖,w: 2.5 mM L-谷氨酰胺,w: 15 mM HEPES,w: 0.5 mM 丙酮酸钠,w: 1.2 g/L NaHCO3(Cytion 文章编号 820400a)。
Incubation atmosphere

37°C, 5%CO2, 加湿环境。

Supplements
在培养基中添加 10% FBS
Dissociation reagent
Accutase
Subculturing
去除粘附细胞上的旧培养基,用不含钙和镁的 PBS 冲洗。T25 烧瓶用 3-5 毫升 PBS,T75 烧瓶用 5-10 毫升。然后用 Accutase 完全覆盖细胞,T25 烧瓶用 1-2 毫升,T75 烧瓶用 2.5 毫升。让细胞在室温下孵育 8-10 分钟,使其分离。孵育后,用 10 毫升培养基轻轻混合细胞使其重悬,然后用 300xg 离心 3 分钟。弃去上清液,用新鲜培养基重悬细胞,并将其转移到已装有新鲜培养基的新烧瓶中。
Seeding density
1 × 10⁴ 个细胞/平方厘米
Fluid renewal
每周 2 至 3 次
Post-thaw recovery
很好。让细胞从冷冻过程中恢复 24 至 48 小时。
Thawing and culturing
  1. Confirm that the vial remains deeply frozen upon delivery, as cells are shipped on dry ice to maintain optimal temperatures during transit.

  2. Upon receipt, either store the cryovial immediately at temperatures below -150°C to ensure the preservation of cellular integrity, or proceed to step 3 if immediate culturing is required.

  3. For immediate culturing, swiftly thaw the vial by immersing it in a 37°C water bath with clean water and an antimicrobial agent, agitating gently for 40-60 seconds until a small ice clump remains.

  4. Perform all subsequent steps under sterile conditions in a flow hood, disinfecting the cryovial with 70% ethanol before opening.

  5. Carefully open the disinfected vial and transfer the cell suspension into a 15 ml centrifuge tube containing 8 ml of room-temperature culture medium, mixing gently.

  6. Centrifuge the mixture at 300 x g for 3 minutes to separate the cells and carefully discard the supernatant containing residual freezing medium.

  7. Gently resuspend the cell pellet in 10 ml of fresh culture medium. For adherent cells, divide the suspension between two T25 culture flasks; for suspension cultures, transfer all the medium into one T25 flask to promote effective cell interaction and growth.

  8. Adhere to established subculture protocols for continued growth and maintenance of the cell line, ensuring reliable experimental outcomes.

07Quality control and cryopreservation

Sterility

使用基于 PCR 的检测方法和基于发光的支原体检测方法排除支原体污染。

为确保没有细菌、真菌或酵母菌污染,每天都要对细胞培养物进行目视检查。

Freeze medium
我们使用完全生长培养基(包括 FBS)+10% DMSO 或 CM-1(Cytion 商品目录编号 800100)作为冷冻保存培养基,以获得足够的解冻后存活率,CM-1(Cytion 商品目录编号 800100)含有优化的渗透保护剂和代谢稳定剂,可提高恢复能力并减少冷冻引起的应激。
Storage conditions

如需长期保存,可将样品瓶放入气相液氮中,温度约为 -150 至 -196 ℃。在-80 °C下保存只能作为转入液氮前的短暂过渡。

Shipping conditions

冷冻保存的细胞系用干冰装运,并用经过验证的隔热包装和足够的制冷剂在整个运输过程中保持约 -78 °C 的温度。收到货后,应立即检查容器,并立即将小瓶转移到适当的储藏室。

08Donor

Breed / subspecies
C57/L