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TOV-112D细胞

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产品名称: TOV-112D细胞
产品型号: TOV-112D
产品展商: HZbscience
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简单介绍

TOV-112D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。TOV-112D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。


TOV-112D细胞  的详细介绍

TOV-112D细胞

生长状态: 贴壁生长

细胞形态: 上皮样

运输方式: 冻存运输

数量: 大量

年限: grade 3, stage IIIC

ATCC Number: CRL-11731™

相关**: 其他**

是否是肿瘤细胞: 1

物种来源: 人

器官来源: 卵巢

Designations: TOV-112D

Depositors: University of Montreal

TOV-112D细胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens deposited as human

Morphology: epithelial


Source: Organ: ovary

Tumor Stage: grade 3, stage IIIC

Disease: primary malignant adenocarcinoma; endometrioid carcinoma

Cellular Products: keratin [49408]

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: Yes

Oncogene: her2/neu +, p53 (mutated, Arg --> His mutation at exon 6, codon 175)

DNA Profile (STR): TOV-112D细胞Amelogenin: X

CSF1PO: 12

D13S317: 8

D16S539: 9,12

D5S818: 10

D7S820: 9,10

THO1: 6

TPOX: 8,11

vWA: 18

Cytogenetic Analysis: 52, XX, add(X)(p22), +add(1)(p22), +add(1)(p22), +2, +9, +12, add(15)(p11), +17 [49408]

Age: 42 years *****

Gender: female

Comments: This cell line was initiated in October of 1992 from a patient with early onset ovarian cancer. The patient was of French-Canadian descent with an unknown family history of ovarian cancer. [49408]

Unlike TOV-21G (ATCC CRL-11730) and OV-90 (ATCC CRL-11732), the TOV-112D cell line does not exhibit a deletion at chromosome 3p24. [42090]

TOV-112D细胞Propagation: ATCC complete growth medium: The base medium for this cell line is a 1:1 mixture of MCDB 105 medium containing a final concentration of 1.5 g/L sodium bicarbonate and Medium 199 containing a final concentration of 2.2 g/L sodium bicarbonate. To make the complete growth medium, add the following components to the base medium:

fetal bovine serum to a final concentration of 15%


Temperature: 37.0°C

Subculturing: Protocol: Remove medium, add fresh 0.05% trypsin - 0.53 mM EDTA, rinse and remove trypsin. Allow the culture sit at room temperature (or 37C) until the cells detach. Add fresh medium, aspirate and dispense into new flasks.

Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:3 is recommended

Medium Renewal: Every 3 to 4 days

Preservation: Freeze medium: Complete growth medium 95%; DMSO, 5%

Storage temperature: liquid nitrogen vapor temperature

Related Products: recommended serum:ATCC 30-2020

purified DNA:ATCC CRL-11731

References: 42090: Mes-Masson AM, Provencher D. Primary cultures of normal and tumoral human ovarian epithelium. US Patent 5,710,038 dated Jan 20 1998

49408: Provencher DM, et al. TOV-112D细胞Characterization of four novel epithelial cancer cell lines. In Vitro Cell. Dev. Biol. Anim. 36: 357-361, 2000. PubMed: 10949993

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