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PG13/LN c8细胞

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  • 产品名称:PG13/LN c8细胞
  • 产品型号:PG13/LN c8
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-08-18
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简单介绍
PG13/LN c8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。PG13/LN c8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。
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PG13/LN c8细胞

是否是肿瘤细胞: 0

物种来源: 小鼠

运输方式: 冻存运输

生长状态: 贴壁生长

品系: NIH/Swiss

细胞形态: 成纤维样

年限: embryo

ATCC Number: CRL-10685™

数量: 大量

相关**: 正常

Designations: PG13/LN c8

PG13/LN c8细胞Depositors: Fred Hutchinson Cancer Res. Cntr.

Biosafety Level: 2 [CELLS CONTAIN RETROVIRUS ]

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

Organism: Mus musculus

Morphology: fibroblast


Source: Disease: normal

Strain: NIH/Swiss

Cellular Products: a Gibbon ape Leukemia Virus (GaLV) based neomycin resistance transducing vector

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. PG13/LN c8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.

Reverse Transcript: positive

Age: embryo

Comments: PG13/LN c8 cells produce a retroviral vector (LN) that transduces the neo gene and can infect cells from many mammalian species (other than mice).

The line was derived from PG13 (see ATCC CRL-10686).

Although virus production has not been observed, there is a possibility that the cells will produce a virus similar to GaLV (a moderate risk oncogenic virus) and Biosafety Level 2 or higher precautions should be taken when using this cell line.

Propagation: ATCC complete growth medium: PG13/LN c8细胞The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Temperature: 37.0°C

Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 is recommended

Medium Renewal: Every 2 to 3 days

Remove medium, add fresh 0.25% Trypsin, 0.02% EDTA solution and allow the flask to sit at room temperature (or 37C) until the cells detach (2 to 3 minutes). PG13/LN c8细胞Add fresh medium, aspirate and dispense into new flasks.

References: 1818: Miller AD, et al. Construction and properties of retrovirus packaging cells based on gibbon ape leukemia virus. J. Virol. 65: 2220-2224, 1991. PubMed: 1850008

4473: Miller AD, Rosman GJ. Improved retroviral vectors for gene transfer and expression. BioTechniques 7: 980-990, 1989. PubMed: 2631796

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