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BHT101
Tissue
甲状腺
Disease
甲状腺无细胞癌
Metastatic site
淋巴结
Synonyms
BHT-101

Documents

BHT101

Cell line · Product number 305112

The BHT101 cell line is derived from the lymph node metastasis of a 63-year-old woman diagnosed with anaplastic papillary thyroid carcinoma. This cell lin...

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

01General information

Description

BHT101 细胞系来自一名 63 岁女性的淋巴结转移灶,她被诊断为无弹性甲状腺乳头状癌。这种细胞系来自一种侵袭性极强的致命性甲状腺癌,以进展迅速和预后不良而闻名。BHT101 细胞的显著特点是缺乏激素分泌,这是甲状腺无弹性癌细胞的典型特征,因为这些细胞往往失去合成甲状腺激素的能力,而这些激素是分化程度较高的甲状腺组织的特征。

在生物标志物表达方面,BHT101 细胞的甲状腺球蛋白和甲状腺素(T4)部分呈阳性。甲状腺球蛋白是一种前体糖蛋白,对甲状腺激素 T3 和 T4 的产生至关重要,通常用作区分甲状腺癌类型的肿瘤标志物。BHT101细胞中存在甲状腺球蛋白,即使只是部分存在,也对甲状腺癌病理学研究和甲状腺癌去分化的分子机制研究具有重要意义。该细胞系的独特特征使其成为研究无性甲状腺癌进展和转移行为的宝贵模型,为研究驱动这些过程的分子改变提供了深入的见解。

Tissue
甲状腺
Disease
甲状腺无细胞癌
Metastatic site
淋巴结
Synonyms
  • BHT-101

02Classification

Organism
Human
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮细胞

04Identifiers

Citation
BHT101(Cytion 产品编号 305112)
NCBI TaxID
9606
Cellosaurus
CVCL_1085

05Handling and culture

Culture medium
EMEM(MEM Eagle),w:2 mM L-谷氨酰胺,w:2.2 g/L NaHCO3,w:EBSS(Cytion 文章编号 820100a)。
Incubation atmosphere

37°C, 5%CO2, 加湿环境。

Supplements
在培养基中添加 20% 热灭活 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

Donor age
63 年
Ethnicity
欧洲