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MC3T3-E1
Tissue
骨,小腿
Synonyms
Mc3T3-E1, MC3T3E1, MC-3T3-E1, MC 3T3-E1

Documents

MC3T3-E1

Cell line · Product number 305187

MC3T3-E1 is a pre-osteoblastic cell line derived from the calvaria of a mouse embryo. These cells are extensively utilized in the study of osteogenesis, p...

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

01General information

Description

MC3T3-E1 是一种前成骨细胞系,来源于小鼠胚胎的小腿。这些细胞被广泛用于成骨研究,特别是用于研究骨形成和分化的分子和细胞机制。MC3T3-E1 细胞系以其在体外分化成成骨细胞的强大能力而闻名,抗坏血酸和 beta-甘油磷酸酯可刺激这一过程。这种分化的标志是碱性磷酸酶、骨钙蛋白和 I 型胶原等关键成骨标志物的表达。

MC3T3-E1 细胞在骨生物学研究(包括骨基质沉积和矿化研究)中发挥着重要作用。这些细胞为研究各种药物、激素和基因修饰对成骨细胞功能和骨形成的影响提供了可靠的模型。此外,MC3T3-E1 细胞系对于研究骨质疏松症和其他骨相关疾病等病理情况也很有价值。MC3T3-E1 细胞系易于培养,对成骨刺激的反应特征明显,是研究人员揭示复杂的骨生理和病理过程的首选。

Tissue
骨,小腿
Applications
体外成骨细胞分化
Synonyms
  • Mc3T3-E1
  • MC3T3E1
  • MC-3T3-E1
  • MC 3T3-E1

02Classification

Organism
Mouse
Sex
Unspecified
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
纤维母细胞样
Cell type
成骨细胞
Tumourigenic
是,在免疫缺陷小鼠中
Doubling time
24 至 48 小时

04Identifiers

Citation
MC3T3-E1(Cytion 目录号 305187)
NCBI TaxID
10090
Cellosaurus
CVCL_0409

05Expression and susceptibility

Products
胶原蛋白

06Handling and culture

Culture medium
α-MEM,w:2.0 mM 稳定谷氨酰胺,w:核糖核苷,w:脱氧核糖核苷,w:1.0 mM 丙酮酸钠,w:2.2g/L NaHCO3,w/o:抗坏血酸(GIBCO,目录号 A1049001。我们不供应该产品,请考虑其他供应商。如需进一步帮助,请告知我们)。
Incubation atmosphere

37°C, 5%CO2, 加湿环境。

Supplements
在培养基中添加 10% 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.

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

Breed / subspecies
C57BL/6
Donor age
1 天