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Ana-1
Tissue
骨髓
Synonyms
ANA-1, ANA1

Documents

Ana-1

Cell line · Product number 305172

The Ana-1 cell line is a murine macrophage cell line derived from the ascites of a BALB/c mouse with a methylcholanthrene-induced tumor. This cell line is...

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

01General information

Description

Ana-1细胞系是一种源自BALB/c小鼠腹水的鼠巨噬细胞系,该小鼠患有甲基胆蒽诱导的肿瘤。由于该细胞系能够产生多种细胞因子,并在先天免疫应答中发挥重要作用,因此在免疫学研究中被广泛应用。 Ana-1细胞具有吞噬活性,并能产生一氧化氮(NO),这对针对病原体和肿瘤细胞的细胞毒性反应至关重要。

此外,Ana-1细胞已被用作研究巨噬细胞活化及免疫应答相关信号通路的模型系统。 这些细胞通过上调促炎细胞因子的表达来响应脂多糖(LPS)的刺激,因此非常适合用于研究炎症和宿主防御系统的分子机制。它们与各种免疫学检测方法的兼容性,也使其在药物筛选以及理解巨噬细胞与免疫系统中其他细胞类型的相互作用方面具有重要价值。

Tissue
骨髓
Synonyms
  • ANA-1
  • ANA1

02Classification

Organism
Mouse
Growth properties
Adherent and suspension
Biosafety level
1

03Characteristics

Morphology
巨噬细胞

04Identifiers

Citation
Ana-1(Cytion 产品编号 305172)
NCBI TaxID
10090
Cellosaurus
CVCL_0142

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% 热灭活 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。
Seeding density
2至4×10⁴个细胞/平方厘米
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
C57BL/6