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NCCIT细胞

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产品名称: NCCIT细胞
产品型号: NCCIT
产品展商: HZbscience
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简单介绍

NCCIT细胞应如何避免细胞污染,细胞污染的种类可分成**、酵母菌、霉菌、病毒和霉浆菌。主要的污染原因为无菌操作技术不当、操作室环境不佳、污染之血清和污染之细胞等。严格之无菌操作技术、清洁的环境、与品质良好之细胞来源和培养基配制是减低污染之*好方法。NCCIT细胞何时须更换培养基?视细胞生长密度而定,或遵照细胞株基本数据上之更换时间,按时更换培养基即可。


NCCIT细胞  的详细介绍

NCCIT细胞

生长状态: 贴壁生长

运输方式: 冻存运输

ATCC Number: CRL-2073™

相关**: 其他**

是否是肿瘤细胞: 1

物种来源: 人

数量: 大量

年限: *****

细胞形态: 上皮样

NCCIT细胞Designations: NCCIT

Depositors: I Damjanov

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Disease: pluripotent embryonal carcinoma; teratocarcinoma

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.

Tumorigenic: NCCIT细胞Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 10,12

D13S317: 11

D16S539: 9,12

D5S818: 10,13

D7S820: 10

THO1: 7,9

TPOX: 8

vWA: 14,18

Age: *****

Gender: male

Ethnicity: Japanese

Comments: NCCIT细胞NCCIT was established by Shinichi Teshima (National Cancer Institute, Tokyo, Japan) in 1985 from a mediastinal mixed germ cell tumor.

This pluripotent stem cell line is capable of somatic and extraembryonic differentiation.

The undifferentiated cells are equivalent to a stage intermediate between seminoma and embryonal carcinoma.

They will differentiate in response to retinoic acid.

NCCIT cells are negative for keratin.

They are positive for vimentin and placental alkaline phosphatase.

The line was contaminated with mycoplasma, but was cured by the depositor prior to deposit at the ATCC .

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%.

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:8 is recommended

Medium Renewal: Add fresh medium at the time of subculture

Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin. Let the culture sit at room temperature (or at 37C) for 2 to 5 minutes. NCCIT细胞Add fresh medium, aspirate and dispense into new flasks. Subculture two times weekly.

Preservation: Culture medium, 95%; DMSO, 5%

References: 22742: Teshima S, et al. Four new human germ cell tumor cell lines. Lab. Invest. 59: 328-336, 1988. PubMed: 2842544

22743: Damjanov I, et al. Retinoic acid-induced differentiation of the developmentally pluripotent human germ cell tumor-derived cell line, NCCIT. Lab. Invest. 68: 220-232, 1993. PubMed: 7680083

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