Skip to content
SK-N-BE(2)
Tissue
大脑
Disease
神经母细胞瘤
Metastatic site
骨髓
Synonyms
SK-N-BE2, SK-N-BE-2, SKNBE(2), SKNBE-2, SKNBE2, SK-N-BE, SKNBE

Documents

SK-N-BE(2)

Cell line · Product number 305058

The cells exhibit moderate levels of dopamine beta hydroxylase activity.SK-N-BE(2) cells have a reported saturation density greater than 1×106 cel...

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

01General information

Description
这些细胞表现出中等水平的多巴胺β-羟化酶活性。SK-N-BE(2)细胞的饱和密度据报道超过1×10⁶个细胞/平方厘米。细胞形态各异,部分细胞具有长突起,另一些则呈上皮样形态。这些细胞会聚集形成团块并悬浮于培养液中。
Tissue
大脑
Disease
神经母细胞瘤
Metastatic site
骨髓
Synonyms
  • SK-N-BE2
  • SK-N-BE-2
  • SKNBE(2)
  • SKNBE-2
  • SKNBE2
  • SK-N-BE
  • SKNBE

02Classification

Organism
Human
Sex
Male
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
神经母细胞
Tumourigenic
是

04Identifiers

Citation
SK-N-BE(2)(Cytion 产品编号 305058)
NCBI TaxID
9606
Cellosaurus
CVCL_0528

05Handling and culture

Culture medium
请按 50:50 的比例混合 EMEM 和 Ham's F12(Cytion 文章编号 820100a 和 820600a)。
Incubation atmosphere

37°C, 5%CO2, 加湿环境。

Supplements
在培养基中添加 10% FBS
Dissociation reagent
Accutase
Subculturing
将悬浮细胞收集到 15 毫升试管中,用不含钙和镁的 PBS(T25 烧瓶用 3-5 毫升,T75 烧瓶用 5-10 毫升)轻轻清洗粘附的细胞。涂抹 Accutase(T25 烧瓶 1-2 毫升,T75 烧瓶 2.5 毫升),确保完全覆盖细胞层。让细胞在室温下孵育 10 分钟。孵育后,将悬浮细胞和粘附细胞混合并离心。离心后,小心重悬细胞团,并将细胞悬浮液转移到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
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
2 年
Ethnicity
欧洲