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HROGas03
Tissue
胃部
Disease
胃腺癌

Documents

HROGas03

Cell line · Product number 300437

The HROGas03 cell line is derived from the gastric adenocarcinoma of an adult female patient. Gastric adenocarcinoma, a common type of stomach cancer, ari...

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Recommended (freshest lot)
  • CoA
1

01General information

Description

HROGas03 细胞系来源于一名成年女性患者的胃腺癌。胃腺癌是一种常见的胃癌,来自胃黏膜的腺上皮细胞,通常预后不良。作为一种模型,HROGas03 为研究胃腺癌的发生、发展和耐药性的分子途径提供了宝贵的资源。供体的年龄相关性,如潜在的基因组不稳定性和肿瘤微环境的改变,可以为研究老年人的癌症生物学提供独特的见解。

这种细胞系使研究人员能够探索驱动胃癌的关键分子机制,如肿瘤抑制基因(如 TP53)的突变、细胞周期的改变和信号通路的失调,包括 Wnt、MAPK 和 PI3K/AKT 通路。这些通路往往与胃癌细胞的生存、增殖和转移潜能有关。HROGas03 细胞系还可用于评估靶向疗法、化疗药物或联合疗法的疗效,从而有可能改进胃癌患者的治疗策略,尤其是老年人群。

Tissue
胃部
Disease
胃腺癌

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent and suspension
Biosafety level
1

03Characteristics

Morphology
上皮样

04Identifiers

Citation
HROGas03(Cytion 目录号 300437)
NCBI TaxID
9606
Cellosaurus
CVCL_2U70

05Handling 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。
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.

06Quality 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
作为冷冻保存培养基,我们使用 50% 基础培养基 + 40% FBS + 10% DMSO 或 CM-1(Cytion 目录号 800100),其中包括优化的渗透保护剂和代谢稳定剂,以促进恢复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。

07Donor

Donor age
80岁
Ethnicity
高加索人