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- NCI-H460 [H460]
- 2025年11月21日
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- 供应商：
复祥生物
- 细胞类型：
普通细胞株-科研实验
- 物种来源：
人
- 运输方式：
常温
- 生长状态：
正常
- 库存：
大量
NCI-H460 [H460] 人大细胞肺癌细胞
1640+10% FBS 。细胞货期8-10个工作日
上海复祥生物提供 ATCC 细胞|细胞系|细胞株|肿瘤细胞|细胞|贴壁细胞|悬浮细胞|,细胞库管理规范,提供的细胞株背景清楚,提供参考文献和培养条件,网站上有细胞照片,欢迎
ATCC® Number: HTB-177™
Designations: NCI-H460 [H460]
Depositors: AF Gazdar, JD Minna
Biosafety Level: 1
Shipped: frozen
Medium & Serum: See Propagation
Growth Properties: adherent
Organism: Homo sapiens (human)
Morphology: epithelial
Source: Organ: lung
Disease: carcinoma; large cell lung cancer
Derived from metastatic site: pleural effusion
Permits/Forms: In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.
Isolation: Isolation date: 1982
Tumorigenic: Yes
DNA Profile (STR): Amelogenin: X,Y
CSF1PO: 11,12
D13S317: 13
D16S539: 9
D5S818: 9,10
D7S820: 9,12
THO1: 9.3
TPOX: 8
vWA: 17
Cytogenetic Analysis: modal numbr = 57; range = 53 to 65.This is a hypotriploid human cell line. The modal chromosome number is 57 although cells with 58 chromosomes occurred with a comparable frequency. The frequency of higher ploidies was 1.7%. Seven marker chromosomes, der(9)t(1;9)(q21;p24), der(9)t(7;9)(p11;p22), t(10q14q), der(16)t(7;16)(q11.23;q22), a small ring (about 1/2 the size of a G chromosome) and two others, were common to all cells. Three other markers were found in some cells only. The markers, t(7;9) and t(7;16) were mostly paired. Normal N9 was , and N7 and N16 had only a single copy per cell. Two copies each of the X and the Y were present in all cells.
Isoenzymes: AK-1, 1
ES-D, 1
G6PD, B
GLO-I, 1-2
Me-2, 1
PGM1, 1
PGM3, 1
Gender: male
Comments: The NCI-H460 cell line was derived by A.F. Gazdar and associates in 1982 from the pleural fluid of a patient with large cell cancer of the lung.
The cells express easily detectable p53 mRNA at levels comparable to normal lung tissue, and exhibit no gross structural DNA abnormalities.
The cells stain positively for keratin and vimentin but are negative for neurofilament triplet protein.
Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Temperature: 37.0°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Subculturing: Protocol:
Remove and discard culture medium.
Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
Add appropriate aliquots of the cell suspension to new culture vessels.
Incubate cultures at 37°C.
Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended
Medium Renewal: Twice per week
Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Doubling Time: 23 hrs in medium with serum; 42 to 60 hrs in serum
Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001
recommended serum:ATCC 30-2020
References: 1605: Banks-Schlegel SP, et al. Intermediate filament and cross-linked envelope expression in human lung tumor cell lines. Cancer Res. 45: 1187-1197, 1985. PubMed: 2578876
1806: Takahashi T, et al. p53: A frequent target for genetic abnormalities in lung cancer. Science 246: 491-494, 1989. PubMed: 2554494
22434: Brower M, et al. Growth of cell lines and clinical specimens of human non-small cell lung cancer in a serum-free defined medium. Cancer Res. 46: 798-806, 1986. PubMed: 3940644
32488: Geiger T, et al. Antitumor activity of a PKC-alpha antisense oligonucleotide in combination with standard chemotherapeutic agents against various human tumors transplanted into nude mice. Anticancer Drug Des. 13: 35-45, 1998. PubMed: 9474241
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文献和实验NCI-H460 人大细胞肺癌细胞
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细胞株名称：NCI-H460 人大细胞肺癌细胞 | |
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培养条件: |
完全培养基：RPMI-1640(GIBCO,货号31800022, 添加NaHCO3 1.5g/L, glucose 2.5g/L, Sodium Pyruvate 0.11g/L)，90%；进口优质胎牛血清，10% |
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传代方法: |
收到细胞后，取出培养瓶在显微镜下观察细胞生长情况。 （一）如果细胞未超过80%汇合度时，用75%酒精喷洒整个瓶身消毒后放到超净台内，严格无菌操作，打开细胞培养瓶，吸出培养液，仅留下10ml培养液在瓶内继续培养。 |
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冻存方法: |
冻存液：90%完全培养液，10%DMSO (现用现配) 储存：液氮储存 |
都是贴壁细胞，在消化传代过程中，步骤如下：倒尽旧的培养液－＞用无血清的培养基清洗一两次－＞加入一定量的胰酶，置于37度培养箱中5--10分钟，使细胞悬浮－＞显微镜下观察，待细胞大部分变圆时，回到超静台－＞加入一定量的含血清的新培养液，以终止胰酶作用－＞反复吹打细胞－＞再置显微镜下观察，直到细胞全部悬浮起来－＞吸出一部分加入新的培养瓶中－＞最后再补充加入一定量新的培养液。注意： 1、吹细胞时尽量多吹边角儿，此处细胞生长的多。2、吸出细胞前要混匀，可以剧烈震荡培养瓶。3、我们用的是DMEM
人头颈部肿瘤AM 人腺样囊性癌细胞（高转移）A2 人腺样囊性癌细胞A83 人腺样囊性癌细胞Hep-2 人喉表皮癌细胞KB 人口腔上皮癌细胞CNE-2Z 人鼻咽癌母系细胞肺癌A549 人肺腺癌细胞801-D 人巨细胞性肺癌细胞肺793 肺腺癌细胞H125 人肺癌细胞NCI-H460 人肺癌细胞LTEP-Sm1 人小细胞肺癌细胞(SCLC)消化系统肿瘤 HT-29 人结肠癌细胞 PC-3 人胰腺癌细胞 SW480 人结肠癌细胞
potential loss and cell cycle arrest》的论文。文章了评估 epicatechin 对 NCI-H2172 非小型细胞肺癌细胞的抗癌作用，重点观测其对自噬细胞死亡、线粒体膜电位 （m） 丧失和细胞周期阻滞的影响。图片来源于 Molecular Medicine Reports 官网然而，就在发表后的第二天，PubPeer 网站上的匿名网友指出，文章 Fig4 中的多个细胞为复制细胞。匿名网友指出，相同颜色圈出的细胞是相同的细胞。图片来源于 PubPeer 官网，相同圈中细胞
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