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MLTC-1
Tissue
睾丸
Disease
小鼠绒毛细胞瘤
Synonyms
mLTC-1, Murine Leydig Tumor Cell line-1

Documents

MLTC-1

Cell line · Product number 305175

The MLTC-1 cell line, derived from murine Leydig tumor cells, retains the hormonal responsiveness of the original tumor. This cell line is particularly va...

US$550.00excl. tax and shipping
In stock
Lot
Recommended (freshest lot)
  • CoA
1

01General information

Description

MLTC-1 细胞系源自小鼠的莱迪格肿瘤细胞,保留了原始肿瘤对激素的反应性。这种细胞系对研究类固醇生成和莱蒂格细胞功能特别有价值。MLTC-1 细胞具有莱德细胞的主要特征,包括存在黄体生成素(LH)受体,这对刺激睾酮的产生至关重要。MLTC-1 细胞对激素治疗的反应与原始肿瘤细胞相似。用人绒毛膜促性腺激素(hCG)、黄体生成素、霍乱毒素、氟化钠和 5'-亚胺二磷酸鸟苷酯处理后,会明显刺激膜腺苷酸环化酶的活性。此外,这些细胞还能对 hCG 产生孕酮反应,这进一步突出了它们在研究激素调节和信号通路方面的作用。MLTC-1 细胞系还被用于毒理学研究,以评估各种物质对莱德细胞功能和类固醇生成的影响,因此是生殖生物学和内分泌学研究的重要工具。

Tissue
睾丸
Disease
小鼠绒毛细胞瘤
Synonyms
  • mLTC-1
  • Murine Leydig Tumor Cell line-1

02Classification

Organism
Mouse
Sex
Male
Growth properties
Adherent
Biosafety level
1

03Characteristics

Morphology
上皮细胞
Tumourigenic
是

04Identifiers

Citation
MLTC-1(Cytion 产品编号 305175)
NCBI TaxID
10090
Cellosaurus
CVCL_3544

05Expression and susceptibility

Receptors expressed
促黄体生成素(HcG)、促黄体生成素(LH
Protein expression
孕酮

06Handling 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,并加入 2.5 g/L 葡萄糖和 10 mM HEPES
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