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產品資料

GP+envAM-12細胞

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產品名稱: GP+envAM-12細胞
產品型號: GP+envAM-12
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

GP+envAM-12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?jié){菌。主要的污染原因為無菌操作技術不當、操作室環(huán)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(huán)境、與品質良好之細胞來源和培養(yǎng)基配制是減低污染之*好方法。GP+envAM-12細胞何時須更換培養(yǎng)基?視細胞生長密度而定,或遵照細胞株基本數(shù)據上之更換時間,按時更換培養(yǎng)基即可。


GP+envAM-12細胞  的詳細介紹

GP+envAM-12細胞

細胞形態(tài): 成纖維樣

數(shù)量: 大量

品系: NIH/Swiss

運輸方式: 凍存運輸

生長狀態(tài): 貼壁生長

年限: embryo

ATCC Number: CRL-9641?

器官來源: 胚胎

細胞類型: 成纖維細胞

是否是腫瘤細胞: 0

物種來源: 小鼠

GP+envAM-12細胞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細胞PubMed: 8755577

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