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GP+envAM-12細(xì)胞

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產(chǎn)品名稱: GP+envAM-12細(xì)胞
產(chǎn)品型號(hào): GP+envAM-12
產(chǎn)品展商: HZbscience
產(chǎn)品文檔: 無相關(guān)文檔

簡(jiǎn)單介紹

GP+envAM-12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?yàn)闊o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。GP+envAM-12細(xì)胞何時(shí)須更換培養(yǎng)基?視細(xì)胞生長(zhǎng)密度而定,或遵照細(xì)胞株基本數(shù)據(jù)上之更換時(shí)間,按時(shí)更換培養(yǎng)基即可。


GP+envAM-12細(xì)胞  的詳細(xì)介紹

GP+envAM-12細(xì)胞

細(xì)胞形態(tài): 成纖維樣

數(shù)量: 大量

品系: NIH/Swiss

運(yùn)輸方式: 凍存運(yùn)輸

生長(zhǎng)狀態(tài): 貼壁生長(zhǎng)

年限: embryo

ATCC Number: CRL-9641?

器官來源: 胚胎

細(xì)胞類型: 成纖維細(xì)胞

是否是腫瘤細(xì)胞: 0

物種來源: 小鼠

GP+envAM-12細(xì)胞Designations: GP+envAM-12

Depositors: Trustees of Columbia University

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus

Morphology: fibroblast


Source: Organ: embryo

Strain: NIH/Swiss

Cell Type: fibroblast

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. GP+envAM-12細(xì)胞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.

Age: embryo

Comments: This line is capable of packaging nucleic acids containing a psi packaging sequence into recombinant amphotropic retrovirus genomes.

It can be used to produce retroviral vectors for delivery of foreign genes into susceptible eukaryotic cells.

The line was established by electroporation into NIH 3T3 cells of two plasmids that separately encode the the env region of a murine amphotropic MuLV and the gag, pol and other sequences needed for viral packaging.

Propagation: GP+envAM-12細(xì)胞ATCC complete growth medium: Dulbecco's modified Eagle's medium, 90%; newborn bovine calf serum, 10%. After 1 to 3 days, add 0.015 mg/ml hypoxanthine, 0.25 mg/ml xanthine, 0.025 mg/ml mycophenolic acid and 0.2 mg/ml hygromycin B

Temperature: 37.0°C

Subculturing: Medium Renewal: Twice per week

Remove medium, add fresh 0.10% trypsin in phosphate buffered saline for 3 to 5 minutes, remove trypsin and let the culture sit at 37C for 10 to 15 minutes. Add fresh medium, aspirate and dispense into new flasks.

References: 22050: Bank A, et al. Retroviral packaging cell lines and process of using same. US Patent 5,278,056 dated Jan 11 1994

32557: Medin JA, et al. Correction in trans for Fabry disease: expression, secretion, and uptake of alpha-galactosidase A in patient-derived cells driven by a high-titer recombinant retroviral vector. Proc. Natl. Acad. Sci. USA 93: 7917-7922, 1996. GP+envAM-12細(xì)胞PubMed: 8755577

滬公網(wǎng)安備 31011702004356號(hào)

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