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產(chǎn)品資料

G355-5細(xì)胞

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產(chǎn)品名稱: G355-5細(xì)胞
產(chǎn)品型號: G355-5
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡單介紹

G355-5細(xì)胞應(yīng)如何避免細(xì)胞污染,細(xì)胞污染的種類可分成**、酵母菌、霉菌、病毒和霉?jié){菌。主要的污染原因為無菌操作技術(shù)不當(dāng)、操作室環(huán)境不佳、污染之血清和污染之細(xì)胞等。嚴(yán)格之無菌操作技術(shù)、清潔的環(huán)境、與品質(zhì)良好之細(xì)胞來源和培養(yǎng)基配制是減低污染之*好方法。G355-5細(xì)胞何時須更換培養(yǎng)基?視細(xì)胞生長密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時間,按時更換培養(yǎng)基即可。


G355-5細(xì)胞  的詳細(xì)介紹

G355-5細(xì)胞

細(xì)胞類型: 其他細(xì)胞類型

運輸方式: 凍存運輸

是否是腫瘤細(xì)胞: 0

物種來源: 貓

生長狀態(tài): 貼壁生長

年限: embryo

數(shù)量: 大量

器官來源: 大腦

ATCC Number: CRL-2033?

G355-5細(xì)胞相關(guān)**: 正常

細(xì)胞形態(tài): 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(xì)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(xì)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(xì)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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