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SK-N-AS細胞

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產品名稱: SK-N-AS細胞
產品型號: SK-N-AS
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

SK-N-AS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、病毒和霉漿菌。主要的污染原因為無菌操作技術不當、操作室環境不佳、污染之血清和污染之細胞等。嚴格之無菌操作技術、清潔的環境、與品質良好之細胞來源和培養基配制是減低污染之*好方法。SK-N-AS細胞何時須更換培養基?視細胞生長密度而定,或遵照細胞株基本數據上之更換時間,按時更換培養基即可。


SK-N-AS細胞  的詳細介紹

SK-N-AS細胞

ATCC Number: CRL-2137?

器官來源: 大腦

相關**: 神經母細胞瘤

細胞形態: 上皮樣

細胞類型: 其他細胞類型

運輸方式: 凍存運輸

是否是腫瘤細胞: 1

物種來源: 人

數量: 大量

年限: 6 years

生長狀態: 貼壁生長

Designations: SK-N-AS

SK-N-AS細胞Depositors: C Helson

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: epithelial


Source: Organ: brain

Disease: neuroblastoma

Derived from metastatic site: bone marrow

Cell Type: neuroblast;

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: 1981

Receptors: insulin-like growth factor I (IGF-I), expressed

Tumorigenic: SK-N-AS細胞Yes

DNA Profile (STR): Amelogenin: X

CSF1PO: 10,12

D13S317: 9

D16S539: 14

D5S818: 11,12

D7S820: 11,13

THO1: 9.3

TPOX: 11,12

vWA: 16,17

Age: 6 years

Gender: female

Ethnicity: Caucasian

Comments: SK-N-AS cells synthesize Insulin-like growth factor II (IFG-II) and IGF-II RNA and possess type I IGF receptors [Pubmed ID: 2547840]. Retinoic acid partially inhibits proliferation, and cells fail to differentiate [Pubmed ID: 1751405]. The cells exhibit low or no MDR1 expression.

Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium:

SK-N-AS細胞O.1 mM Non-Essential Amino Acids (NEAA)

fetal bovine serum to a final concentration of 10%


Temperature: 37.0°C

Subculturing: Protocol: Remove spent medium, add fresh 0.25% trypsin, 0.53 MM EDTA solution, rinse and remove trypsin. Let the culture sit at room temperature (or at 37C) until the cells detach. Add fresh medium, aspirate and dispense into new flasks.

Subcultivation Ratio: A subcultivation ratio of 1:5 to 1:10 is recommended

Medium Renewal: Twice per week

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

Storage temperature: liquid nitrogen vapor phase

Doubling Time: 39 hrs

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002

recommended serum:ATCC 30-2020

References: 22290: Sugimoto T, et al. Determination of cell surface membrane antigens common to both human neuroblastoma and leukemia-lymphoma cell lines by a panel of 38 monoclonal antibodies. J. Natl. Cancer Inst. 73: 51-57, 1984. PubMed: 6610792

22439: Iavarone A, et al. Uptake and storage of m-iodobenzylguanidine are frequent neuronal functions of human neuroblastoma cell lines. Cancer Res. 53: 304-309, 1993. PubMed: 8417824

22444: Gaetano C, et al. Retinoic acid negatively regulates p34cdc2 expression during human neuroblastoma differentiation. Cell Growth Differ. 2: 487-493, 1991. PubMed: 1751405

22500: El-Badry OM, et al. SK-N-AS細胞Autonomous growth of a human neuroblastoma cell line is mediated by insulin-like growth factor II. J. Clin. Invest. 84: 829-839, 1989. PubMed: 2547840

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