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IGR-1 细胞
Tissue
皮肤
Disease
恶性黑色素瘤
Metastatic site
腹股沟淋巴结
Synonyms
IGR 1, IGR1, Institut Gustave Roussy-1

Documents

IGR-1 细胞

Cell line · Product number 300219

The IGR-1 cell line is derived from a human malignant melanoma, making it a valuable model for studying the pathophysiology of melanoma and testing anti-c...

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

01General information

Description

IGR-1 细胞系来源于人类恶性黑色素瘤,是研究黑色素瘤病理生理学和测试抗癌疗法的宝贵模型。这些细胞是上皮细胞,具有侵袭性黑色素瘤的典型特征,包括快速增殖和在软琼脂中形成菌落的能力,这是致癌转化的标志。IGR-1 细胞系特别适用于了解黑色素瘤进展的分子机制的研究,以及靶向疗法和免疫疗法的开发和测试。

IGR-1细胞携带黑色素瘤常见的突变,包括MAPK/ERK通路的改变,这种通路在这种癌症类型中经常失调。这些突变导致细胞系能够不受控制地增殖并抵抗细胞凋亡。研究人员利用 IGR-1 细胞来研究各种抑制剂对该信号通路的影响,从而为潜在的治疗策略提供启示。此外,该细胞系表达黑色素瘤相关抗原,因此适合研究针对黑色素瘤的免疫反应,包括开发新型免疫治疗方法。

Tissue
皮肤
Disease
恶性黑色素瘤
Metastatic site
腹股沟淋巴结
Synonyms
  • IGR 1
  • IGR1
  • Institut Gustave Roussy-1

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
多边形
Tumourigenic
是的,在裸鼠身上。

04Identifiers

Citation
IGR-1(Cytion 目录号 300219)
NCBI TaxID
9606
Cellosaurus
CVCL_1303

05Expression and susceptibility

Mutational profile
IGR-1 细胞携带杂合子 BRAFV600K 突变,但它们是 BRAFV600E 的野生型。
Products
黑色素

06Handling and culture

Culture medium
DMEM,w:4.5 克/升葡萄糖,w:4 毫摩尔 L-谷氨酰胺,w:3.7 克/升 NaHCO3,w:1.0 毫摩尔丙酮酸钠(Cytion 编号 820300a)。
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
解冻后为3×10⁴/cm²,常规分裂时为1至2×10⁴/cm²
Fluid renewal
每周 2 至 3 次
Post-thaw recovery
1 至 2 天
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

Donor age
42 年