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產品資料

G355-5細胞

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產品名稱: G355-5細胞
產品型號: G355-5
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

G355-5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。G355-5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。


G355-5細胞  的詳細介紹

G355-5細胞

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: 0

物種來源: 貓

生長狀態: 貼壁生長

年限: embryo

數量: 大量

器官來源: 大腦

ATCC Number: CRL-2033?

G355-5細胞相關**: 正常

細胞形態: 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細胞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細胞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細胞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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