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HMy2
Tissue
造血
Disease
浆细胞白血病
Synonyms
LICR-Lon-HMy-2, LICR-LON-HMy2, LICR.LON.HMy2, Licr.Lon.Hmy2, LICRLON/My2, HMy.2 B, LICR-2

Documents

HMy2

Cell line · Product number 302008

The HMy2 cell line is a human B lymphoblastoid cell line derived from an adult individual. This cell line was originally established for the study of huma...

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

01General information

Description

HMy2 细胞系是一种人 B 淋巴母细胞细胞系,来源于一个成年人。该细胞系最初是为研究人类 B 细胞功能、淋巴瘤和免疫反应而建立的。HMy2 细胞能产生多种免疫球蛋白和细胞因子,是研究 B 细胞活化、分化和淋巴恶性肿瘤分子机制的绝佳模型。

HMy2 细胞表现出 B 淋巴母细胞的典型特征,如核与细胞质比率高,存在表明 B 细胞系的表面标志物,包括 CD19 和 CD20。众所周知,这些细胞还能表达 HLA-DR 抗原,因此适合进行与抗原呈递和免疫反应调节相关的研究。研究人员经常在涉及基因表达、转染和杂交瘤技术的实验中使用 HMy2 细胞,从而推动了治疗性抗体开发和癌症免疫疗法的发展。

Tissue
造血
Disease
浆细胞白血病
Applications
杂交瘤融合伴侣、B 细胞表面抗原分析、细胞毒性药物测试、突变分析、细胞凋亡机制分析、HLA 标准。
Synonyms
  • LICR-Lon-HMy-2
  • LICR-LON-HMy2
  • LICR.LON.HMy2
  • Licr.Lon.Hmy2
  • LICRLON/My2
  • HMy.2 B
  • LICR-2

02Classification

Organism
Human
Sex
Female
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
圆形电池
Cell type
淋巴母细胞
Karyotype
46、低二倍体

04Identifiers

Citation
HMy2(Cytion 目录号 302008)
NCBI TaxID
9606
Cellosaurus
CVCL_8119

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 × 10⁵ 个细胞/毫升
Fluid renewal
每 3 至 5 天
Post-thaw recovery
快速
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
33 年
Ethnicity
高加索人