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GP+E-86细胞

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产品名称: GP+E-86细胞
产品型号: GP+E-86
产品展商: HZbscience
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简单介绍

GP+E-86细胞应如何避免细胞污染,细胞污染的种类可分成**、酵母菌、霉菌、病毒和霉浆菌。主要的污染原因为无菌操作技术不当、操作室环境不佳、污染之血清和污染之细胞等。严格之无菌操作技术、清洁的环境、与品质良好之细胞来源和培养基配制是减低污染之*好方法。GP+E-86细胞何时须更换培养基?视细胞生长密度而定,或遵照细胞株基本数据上之更换时间,按时更换培养基即可。


GP+E-86细胞  的详细介绍

GP+E-86细胞

品系: NIH/Swiss

细胞形态: 成纤维样

数量: 大量

生长状态: 贴壁生长

运输方式: 冻存运输

年限: embryo

器官来源: 胚胎

细胞类型: 成纤维细胞

ATCC Number: CRL-9642™

是否是肿瘤细胞: 0

GP+E-86细胞物种来源: 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细胞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细胞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细胞Retroviral packaging cell lines and process of using same. US Patent 5,278,056 dated Jan 11 1994

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