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GP+E-86細胞

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產品名稱: GP+E-86細胞
產品型號: GP+E-86
產品展商: HZbscience
產品文檔: 無相關文檔

簡單介紹

GP+E-86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。GP+E-86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。


GP+E-86細胞  的詳細介紹

GP+E-86細胞

品系: NIH/Swiss

細胞形態: 成纖維樣

數量: 大量

生長狀態: 貼壁生長

運輸方式: 凍存運輸

年限: embryo

器官來源: 胚胎

細胞類型: 成纖維細胞

ATCC Number: CRL-9642?

是否是腫瘤細胞: 0

GP+E-86細胞物種來源: 小鼠

Designations: GP+E-86

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: GP+E-86細胞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.

Applications: transfection host (Roche Transfection Reagents)

Age: embryo

Comments: This line is capable of packaging nucleic acids containing a psi packaging sequence into recombinant ecotropic 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 of two plasmids into NIH 3T3 cells.

One plasmid contained the gag and pol regions of Moloney murine leukemia virus (Mo-MuLV), the other contained the env region of Mo-MuLV.

Propagation: GP+E-86細胞ATCC complete growth medium: Dulbecco's modified Eagle's medium with 0.015 mg/ml hypoxanthine, 0.25 mg/ml xanthine, and 0.025 mg/ml mycophenolic acid; 90% calf serum, 10%.

Temperature: 37.0°C

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:5 to 1:10 is recommended

Medium Renewal: Twice per week

Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach.

Add fresh culture medium, aspirate and dispense into new culture flasks.

Preservation: culture medium 95%; DMSO, 5%

References: 22050: Bank A, et al. GP+E-86細胞Retroviral packaging cell lines and process of using same. US Patent 5,278,056 dated Jan 11 1994

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