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Y3-Ag 1.2.3
Tissue
浆细胞瘤、骨髓瘤
Disease
大鼠浆细胞骨髓瘤
Synonyms
Y3.AG.1.2.3, Y3-Ag1.2.3, Y3-Ag1, 2, 3, Y3Ag1.2.3, Y-3-Ag 1.2.3, 210-RC Y3-Ag 1, 2, 3, 210RCY3-Ag1.2.3, 210RCY3-Ag123, Y3-Ag123, Y3, Y3M

Documents

Y3-Ag 1.2.3

Cell line · Product number 305207

This cell line is derived from an azaguanine-resistant mutant of S210 myeloma. The cells are resistant to 8-azaguanine but sensitive to HAT. The cells can be...

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

01General information

Description
这种细胞系来源于 S210 骨髓瘤的氮杂鸟嘌呤抗性突变体。这种细胞对 8-氮杂鸟嘌呤具有抗性,但对 HAT 敏感。该细胞可用作制备大鼠-大鼠杂交瘤的大鼠 B 细胞融合伙伴。商业使用或第三方分发须经 C. Milstein 许可。
Tissue
浆细胞瘤、骨髓瘤
Disease
大鼠浆细胞骨髓瘤
Synonyms
  • Y3.AG.1.2.3
  • Y3-Ag1.2.3
  • Y3-Ag1
  • 2
  • 3
  • Y3Ag1.2.3
  • Y-3-Ag 1.2.3
  • 210-RC Y3-Ag 1
  • 2
  • 3
  • 210RCY3-Ag1.2.3
  • 210RCY3-Ag123
  • Y3-Ag123
  • Y3
  • Y3M

02Classification

Organism
Rat
Growth properties
Suspension
Biosafety level
1

03Characteristics

Morphology
淋巴母细胞

04Identifiers

Citation
Y3-Ag 1.2.3(Cytion 产品编号 305207)
NCBI TaxID
10116
Cellosaurus
CVCL_4342

05Expression and susceptibility

Protein expression
免疫球蛋白

06Handling and culture

Culture medium
DMEM,w:4.5 克/升葡萄糖,w:4 毫摩尔 L-谷氨酰胺,w:3.7 克/升 NaHCO3,w:1.0 毫摩尔丙酮酸钠(Cytion 编号 820300a)。
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。
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
LOU/C