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RAW 264.7 gamma NO(-)细胞

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  • 产品名称:RAW 264.7 gamma NO(-)细胞
  • 产品型号:RAW 264.7 gamma NO(-)
  • 产品展商:HZbscience
  • 产品文档:无相关文档
  • 发布时间:2018-06-21
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简单介绍
RAW 264.7 gamma NO(-)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。RAW 264.7 gamma NO(-)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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RAW 264.7 gamma NO(-)细胞


品系: BALB/c

运输方式: 冻存运输

生长状态: 贴壁生长

是否是肿瘤细胞: 0

物种来源: 小鼠

ATCC Number: CRL-2278™

数量: 大量

Designations: RAW 264.7 gamma NO(-)

Depositors: SW Russell

Biosafety Level: 2

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: adherent

RAW 264.7 gamma NO(-)细胞Organism: Mus musculus

Morphology:

Source: Strain: BALB/c

Cellular Products: lysozyme

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. 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.

Receptors: complement (C3), expressed

Antigen Expression: H-2d

Gender: male

Comments: RAW 264.7 gamma NO(-) was derived from the RAW 264.7 (see ATCC TIB-71) mouse monocyte/macrophage cell line ordinally obtained in 1978 from Dr. Peter Ralph.

The cells were not intentionally cloned but were serendipitously obtained during routine culture.

Unlike the parental line, RAW 264.7 gamma NO(-) does not produce nitric oxide upon treatment with interferon gamma alone, but requires LPS for full activation (the iNOS promoter linked to a luciferase reporter gene is also unresponsive to IFN- alone).

This property makes its behavior more like that of normal macrophages from some commonly used strains of mice (e.g. C3H/HeN).

Propagation: RAW 264.7 gamma NO(-)细胞ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.

Atmosphere: air, 95%; carbon dioxide (CO2), 5%

Temperature: 37.0°C

Subculturing: Protocol: Cells can be grown as a monolayer or in spinner cultures. For routine passage cells should be grown on bacterial grade culture dishes. Subcultures are prepared by scraping cells from floor of dishes every two days and diluting to 1 x 10(6) cells/20ml (3 x 10(5) cells/20ml for weekend passage). Cells grown in spinner flasks are inoculated at a density of 1 x 10(5) cells/ml. Spinner culture cell densities should not be allowed to rise above 6 x 10(5) cells/ml.

RAW 264.7 gamma NO(-)细胞Medium Renewal: 2 to 3 times per week

Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO

Storage temperature: liquid nitrogen vapor phase

Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001

recommended serum:ATCC 30-2020

parental cell line:ATCC TIB-71

References: 1135: Ralph P, Nakoinz I. Antibody-dependent killing of erythrocyte and tumor targets by macrophage-related cell lines: enhancement by PPD and LPS. J. RAW 264.7 gamma NO(-)细胞Immunol. 119: 950-954, 1977. PubMed: 894031

1207: Raschke WC, et al. Functional macrophage cell lines transformed by Abelson leukemia virus. Cell 15: 261-267, 1978. PubMed: 212198

22778: Alley EW, et al. A classical enhancer element responsive to both lipopolysaccharide and interferon-gamma augments induction of the iNOS gene in mouse macrophages. Gene 158: 247-251, 1995. PubMed: 7541763

23410: Lorsbach RB, et al. Expression of the nitric oxide synthase gene in mouse macrophages activated for tumor cell killing. Molecular basis for the synergy between interferon-gamma and lipopolysaccharide. J. Biol. Chem. 268: 1908-1912, 1993. PubMed: 7678412


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