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TOV-112D細胞

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產(chǎn)品名稱: TOV-112D細胞
產(chǎn)品型號: TOV-112D
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關文檔

簡單介紹

TOV-112D細胞應如何避免細胞污染,細胞污染的種類可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因為無菌操作技術不當、操作室環(huán)境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環(huán)境、與品質良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。TOV-112D細胞何時須更換培養(yǎng)基?視細胞生長密度而定,或遵照細胞株基本數(shù)據(jù)上之更換時間,按時更換培養(yǎng)基即可。


TOV-112D細胞  的詳細介紹

TOV-112D細胞

生長狀態(tài): 貼壁生長

細胞形態(tài): 上皮樣

運輸方式: 凍存運輸

數(shù)量: 大量

年限: grade 3, stage IIIC

ATCC Number: CRL-11731?

相關**: 其他**

是否是腫瘤細胞: 1

物種來源: 人

器官來源: 卵巢

Designations: TOV-112D

Depositors: University of Montreal

TOV-112D細胞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細胞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細胞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細胞Characterization of four novel epithelial cancer cell lines. In Vitro Cell. Dev. Biol. Anim. 36: 357-361, 2000. PubMed: 10949993

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