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BE(2)-M17細胞

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產品名稱: BE(2)-M17細胞
產品型號: BE(2)-M17
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

BE(2)-M17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。BE(2)-M17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。


BE(2)-M17細胞  的詳細介紹

BE(2)-M17細胞

器官來源: 大腦

數量: 大量

生長狀態: 貼壁生長

年限: 2 years

細胞形態: 神經母細胞

是否是腫瘤細胞: 1

物種來源: 人

ATCC Number: CRL-2267?

運輸方式: 凍存運輸

相關**: 神經母細胞瘤

Designations: BE(2)-M17

Depositors: JL Biedler

BE(2)-M17細胞Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Homo sapiens

Morphology: neuroblast


Source: Organ: brain

Disease: neuroblastoma

Derived from metastatic site: bone marrow

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.

Restrictions: Note: BE(2)-M17 was deposited at the ATCC by June L. Biedler, Memorial Sloan-Kettering Cancer Center. BE(2)-M17 is distributed for academic research purposes only. Memorial Sloan-Kettering releases the line subject to the following: 1.)BE(2)-M17 or its products must not be distributed to third parties. BE(2)-M17細胞Commercial interests are the exclusive property of Memorial Sloan-Kettering Cancer Center. 2.) Any proposed commercial use of BE(2)-M17 including any use by a for-profit entity must first be negotiated with Director, Office of Industrial Affairs, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021; phone (212) 639-6181; FAX (212) 717-3439.

Applications: transfection host (Roche Transfection Reagents)

DNA Profile (STR): Amelogenin: X

CSF1PO: 10

D13S317: 11

D16S539: 11

D5S818: 12

D7S820: 9,10

THO1: 6

TPOX: 8,11

vWA: 18

Age: 2 years

Gender: male

Comments: BE(2)-M17細胞BE(2)-M17 is a clone of the SK-N-BE(2) neuroblastoma cell line (see ATCC CRL-2271) that was established in November of 1972 from a bone marrow biopsy taken from a 2 year old male with disseminated neuroblastoma.

After repeated courses of chemotherapy and radiotherapy.

BE(2)-M17 cells have a reported saturation density of greater than 1 X 10 exp6 cells/sq cm.

The cells grow as multilayering, neuroblastic cells with occasionally long neuritic processes.

As cultures age, cells will aggregate and float.

Propagation: ATCC complete growth medium: The base medium for this cell line is a 1:1 mixture of ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003, and F12 Medium. 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 1:20 to 1:50 is recommended

Medium Renewal: Every 4 to 7 days

Remove spent medium, add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin.

Add fresh trypsin solution (1 to 2 ml) and let the culture sit at room temperature (or at 37C) until the cells detach.

Add fresh medium, aspirate and dispense into new flasks.

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

Doubling Time: 20 to 24 hrs

Related Products: BE(2)-M17細胞recommended serum:ATCC 30-2020

滬公網安備 31011702004356號

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