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MA-CLS-2 细胞
Tissue
乳房
Disease
导管癌
Metastatic site
胸腔积液
Synonyms
MACLS-2, MACLS2

Documents

MA-CLS-2 细胞

Cell line · Product number 300271

The MA-CLS-2 cell line was established from the pleural effusion of a female patient diagnosed with breast ductal carcinoma. This cell line originates fro...

US$650.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
1

01General information

Description

MA-CLS-2 细胞系是根据一名女性乳腺导管癌患者的胸腔积液建立的。该细胞系来源于人类乳腺肿瘤,特别代表了通常与癌症晚期相关的胸膜转移。原始肿瘤被归类为 pT1 NO GII,表明原发肿瘤大小有限(T1),无区域淋巴结转移(N0),并被分级为中度分化(GII)。这些特征表明,肿瘤处于相对早期,但已经扩散到胸膜腔,这种并发症对患者的预后有很大影响。

MA-CLS-2 对研究乳腺癌的转移过程特别有价值,尤其是涉及胸腔积液的转移过程,它可以帮助人们深入了解肿瘤扩散的机制和潜在的治疗靶点。该细胞系为研究转移性乳腺癌细胞与胸膜环境之间的相互作用提供了一个模型,有助于研究旨在预防或治疗转移性疾病的新型干预措施。作为一种来源于导管癌的胸膜转移模型,MA-CLS-2 还可以用于研究转移性乳腺癌的药物反应。

Tissue
乳房
Disease
导管癌
Metastatic site
胸腔积液
Synonyms
  • MACLS-2
  • MACLS2

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮样
Tumourigenic
是,在裸鼠身上
Ploidy status
非整倍体

04Identifiers

Citation
MA-CLS-2(Cytion 目录号 300271)
NCBI TaxID
9606
Cellosaurus
CVCL_4571

05Handling and culture

Culture medium
RPMI 1640,w:2.0 mM 稳定谷氨酰胺,w:2.0 g/L NaHCO3(Cytion 文章编号 820700a)。
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
2 × 10⁴ 个细胞/平方厘米
Fluid renewal
每周 2 至 3 次
Post-thaw recovery
快速
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
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。

07Donor

Donor age
47 年
Ethnicity
高加索人