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GP+envAM-12细胞

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产品名称: GP+envAM-12细胞
产品型号: GP+envAM-12
产品展商: HZbscience
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简单介绍

GP+envAM-12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+envAM-12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+envAM-12细胞  的详细介绍

GP+envAM-12细胞

细胞形态: 成纤维样

数量: 大量

品系: NIH/Swiss

运输方式: 冻存运输

生长状态: 贴壁生长

年限: embryo

ATCC Number: CRL-9641™

器官来源: 胚胎

细胞类型: 成纤维细胞

是否是肿瘤细胞: 0

物种来源: 小鼠

GP+envAM-12细胞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细胞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细胞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细胞PubMed: 8755577

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