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EMT6
Tissue
乳房
Disease
小鼠乳腺恶性肿瘤
Synonyms
EMT-6, Experimental Mammary Tumour-6

Documents

EMT6

Cell line · Product number 305159

The EMT6 cell line is a murine mammary adenocarcinoma line that is extensively used in cancer research, particularly in studies related to breast cancer. ...

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

01General information

Description

EMT6 细胞系是一种小鼠乳腺腺癌细胞系,广泛用于癌症研究,尤其是与乳腺癌有关的研究。EMT6 细胞源自 BALB/c 小鼠的自发性肿瘤,可用于体外和体内分析肿瘤发生、转移和化疗耐药性。这种细胞的特点是在移植到免疫功能健全的小鼠体内后能迅速形成肿瘤,因此是研究肿瘤免疫和抗癌疗法疗效的理想模型。

EMT6 细胞对各种生长条件的适应性很强,有丝分裂指数相对较高,便于在实验室环境中进行培养和实验操作。由于它们对辐射具有明显的敏感性,因此也被用于放射生物学研究,为了解癌症放射治疗的细胞机制提供了帮助。该细胞系在缺氧细胞增敏剂方案的开发中发挥了重要作用,并被用于测试光动力疗法药物的疗效。

Tissue
乳房
Disease
小鼠乳腺恶性肿瘤
Synonyms
  • EMT-6
  • Experimental Mammary Tumour-6

02Classification

Organism
Mouse
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮细胞

04Identifiers

Citation
EMT6(Cytion 产品编号 305159)
NCBI TaxID
10090
Cellosaurus
CVCL_1923

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。
Fluid renewal
每周 2 至 3 次
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

Breed / subspecies
BALB/cCRGL