Skip to content
LS-CLS
Tissue
造血
Disease
淋巴肉瘤

Documents

LS-CLS

Cell line · Product number 603390

The LS-CLS cell line was established from the primary lymphosarcoma of an adult Mesocricetus auratus (hamster). This cell line originates from the hematop...

US$395.00excl. tax and shipping
Made to order
1

01General information

Description

LS-CLS 细胞系是根据成年仓鼠(Mesocricetus auratus)的原发性淋巴肉瘤建立的。淋巴肉瘤是一种影响淋巴细胞的癌症,淋巴细胞是免疫系统的关键组成部分。淋巴肉瘤是典型的恶性肿瘤,增殖迅速,并能转移到各种器官,因此在癌症生物学,尤其是血液系统恶性肿瘤的相关研究中具有重要意义。

作为一种体外模型,LS-CLS 细胞系对研究淋巴肉瘤的发生和发展机制很有价值。它还可用于研究潜在的治疗方法,包括针对造血癌症的化疗药物和靶向疗法。

Tissue
造血
Disease
淋巴肉瘤

02Classification

Organism
Golden hamster
Sex
Unspecified
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
圆形电池

04Identifiers

Citation
LS-CLS(Cytion 目录号 603390)
NCBI TaxID
10036
Cellosaurus
CVCL_5789

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
Subculturing
通过定期添加或更换培养基来维持细胞培养。初始培养时细胞密度应为5×10⁵个细胞/毫升,并保持细胞浓度在3×10⁵至1×10⁶个细胞/毫升范围内以获得最佳生长效果。
Seeding density
1至2×10⁶个细胞/毫升
Fluid renewal
每 3 至 5 天
Post-thaw recovery
24 至 48 小时
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
成人