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平臺(tái)編號(hào)：bio-68213
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國(guó)際編號(hào)：CRL-2278™
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細(xì)胞信息： RAW 264.7 gamma NO-
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規(guī)格：frozen
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用途：ATCC原裝細(xì)胞
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服務(wù)費(fèi)用：
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注意事項(xiàng)：僅用于科學(xué)研究或者工業(yè)應(yīng)用等非醫(yī)療目的不可用于人類或動(dòng)物的臨床診斷或治療，非藥用，非食用（產(chǎn)品信息以出庫(kù)為準(zhǔn)）
RAW 264.7 gamma NO(-)
品系：BALB/c
運(yùn)輸方式：凍存運(yùn)輸
生長(zhǎng)狀態(tài)：貼壁生長(zhǎng)
是否是腫瘤細(xì)胞：0
物種來(lái)源：小鼠
ATCC Number：CRL-2278?
數(shù)量：大量
規(guī)格：0.5ml Designations: RAW 264.7 gamma NO(-)
Depositors: ?SW Russell
Biosafety Level:2
Shipped: frozen
Medium & Serum: See Propagation Growth Properties:adherent
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: 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.
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. 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
