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BE(2)-M17细胞

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产品名称: BE(2)-M17细胞
产品型号: BE(2)-M17
产品展商: HZbscience
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简单介绍

BE(2)-M17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。BE(2)-M17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。


BE(2)-M17细胞  的详细介绍

BE(2)-M17细胞

器官来源: 大脑

数量: 大量

生长状态: 贴壁生长

年限: 2 years

细胞形态: 神经母细胞

是否是肿瘤细胞: 1

物种来源: 人

ATCC Number: CRL-2267™

运输方式: 冻存运输

相关**: 神经母细胞瘤

Designations: BE(2)-M17

Depositors: JL Biedler

BE(2)-M17细胞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细胞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细胞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细胞recommended serum:ATCC 30-2020

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