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MDCC-MSB1
Disease
马雷克病
Synonyms
MDCC MSB1, MDCC-MSB-1, MSB-1, MSB1

Documents

MDCC-MSB1

Cell line · Product number 601413

The MDCC-MSB1 cell line is a lymphoblastoid cell line derived from a chicken with Marek's disease, a highly contagious viral disease caused by Marek's dis...

US$800.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

马立克氏病是由马立克氏病病毒(MDV)引起的一种高度传染性的病毒性疾病,属于疱疹病毒科。这些细胞被广泛用于兽医病毒学和免疫学研究,以研究 MDV 的发病机制,以及开发和评估针对这种疾病的疫苗。MDCC-MSB1 细胞系具有淋巴细胞的典型特征,如表达特异性表面标志物和产生细胞因子,这对了解 MDV 感染的免疫反应至关重要。

除了在 MDV 研究中的作用外,MDCC-MSB1 细胞系对于研究禽类肿瘤发生和病毒复制的一般机制也很有价值。这种细胞在悬浮培养中生长旺盛,便于大规模生产和实验操作。研究人员利用这种细胞系研究 MDV 与宿主之间的分子相互作用,确定参与疾病进展的病毒和宿主因素,并筛选潜在的抗病毒化合物。总之,MDCC-MSB1 细胞系是禽病毒学基础研究和应用研究的重要工具。

Disease
马雷克病
Synonyms
  • MDCC MSB1
  • MDCC-MSB-1
  • MSB-1
  • MSB1

02Classification

Organism
Chicken
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
圆形电池
Cell type
淋巴母细胞
Doubling time
10 小时

04Identifiers

Citation
MDCC-MSB1(Cytion 目录编号 601413)
NCBI TaxID
9031
Cellosaurus
CVCL_4542

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 × 10⁶ 个细胞/毫升
Fluid renewal
每周 2 至 3 次
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.

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。