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AS-30D
Tissue
肝脏
Disease
肝细胞癌
Synonyms
A-S-30D, AS30D

Documents

AS-30D

Cell line · Product number 500116

Established in vitro from the AS-30D tumor ascites.

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

01General information

Description
由 AS-30D 肿瘤腹水在体外建立。
Tissue
肝脏
Disease
肝细胞癌
Synonyms
  • A-S-30D
  • AS30D

02Classification

Organism
Rat
Sex
Female
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
圆形细胞,松散粘附,漂浮
Tumourigenic
是的,在 Sprague-Dawley 大鼠中
Karyotype
大鼠下二倍体核型,12%为四倍体,第 38 期(35-41)。
Doubling time
26 小时

04Identifiers

Citation
AS-30D(Cytion 目录编号 500116)
NCBI TaxID
10116
Cellosaurus
CVCL_1949

05Expression and susceptibility

Viruses
RAP 测试:阴性。

06Handling 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
通过上下吸取操作轻柔匀化烧瓶中的细胞悬液,随后取代表性样本测定每毫升细胞密度。用新鲜培养基将悬液稀释至1×10⁵细胞/毫升浓度,并将调整后的悬液分装至新烧瓶中进行后续培养。
Seeding density
建议的接种密度为1×10⁶个细胞/毫升。
Fluid renewal
每 3 至 5 天
Post-thaw recovery
解冻后,让细胞从冷冻过程中恢复至少 24 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.

07Quality 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。

08Donor

Donor age
16 个月