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G355-5细胞

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产品名称: G355-5细胞
产品型号: G355-5
产品展商: HZbscience
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简单介绍

G355-5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。G355-5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。


G355-5细胞  的详细介绍

G355-5细胞

细胞类型: 其他细胞类型

运输方式: 冻存运输

是否是肿瘤细胞: 0

物种来源: 猫

生长状态: 贴壁生长

年限: embryo

数量: 大量

器官来源: 大脑

ATCC Number: CRL-2033™

G355-5细胞相关**: 正常

细胞形态: 其他

Designations: G355-5

Depositors: KJ Dunn

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Felis catus

Morphology: glial, astrocyte


Source: Organ: brain

Disease: normal

G355-5细胞Cell Type: astrocyte;

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.

Virus Susceptibility: xenotropic murine leukemia virus; amphotropic murine leukemia virus; mink cell focus forming (MCF) virus; RD-114 virus; feline leukemia virus (FeLV) A, B, C; baboon endogenous virus (BaEV); macaque virus;

simian sarcoma associated virus (SSAV); feline immunodeficiency virus (34TF10)

Age: embryo

Comments: This is a cloned derivative of the G355 cell line originally produced and distributed by the Naval Biosciences Laboratory.

The line is useful for generating stocks of various C type retroviruses.

Propagation: G355-5细胞ATCC complete growth medium: The base medium for this cell line is ATCC-formulated McCoy's 5a Medium Modified, Catalog No. 30-2007. To make the complete growth medium, add the following components to the base medium:

heat-inactivated fetal bovine serum to a final concentration of 10%

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:5 is recommended

Medium Renewal: 2 to 3 times per week

Remove medium, and rinse the monolayer with fresh 0.25% trypsin, 0.03% EDTA solution.

Remove the trypsin, add fresh trypsin (1 to 2 ml) and let the culture sit at room temperature (or at 37C) until the cells detach (about 10 minutes).

Add fresh medium, aspirate and dispense into new flasks.

References: 22563: Haapala DK, et al. G355-5细胞Isolation from cats of an endogenous type C virus with a novel envelope glycoprotein. J. Virol. 53: 827-833, 1985. PubMed: 2983093

22991: Bassin RH, et al. Normal DBA/2 mouse cells synthesize a glycoprotein which interferes with MCF virus infection. Virology 123: 139-151, 1982. PubMed: 6959413

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