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        1. 上海復(fù)祥生物科技有限公司

          當(dāng)前位置:> 供求商機(jī)> RAW 264.7小鼠單核巨噬細(xì)胞白血病細(xì)胞

          [供應(yīng)]RAW 264.7小鼠單核巨噬細(xì)胞白血病細(xì)胞

          貨物所在地:上海上海市

          更新時(shí)間:2024-07-11 21:00:05

          有效期:2024年7月11日 -- 2025年1月11日

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          RAW 264.7小鼠單核巨噬細(xì)胞白血病細(xì)胞,原代細(xì)胞|細(xì)胞系|細(xì)胞株|菌種;細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和*培養(yǎng)條件!
          RAW 264.7小鼠單核巨噬細(xì)胞白血病細(xì)胞 的詳細(xì)介紹

          RAW 264.7小鼠單核巨噬細(xì)胞白血病細(xì)胞
          ATCC® Number:  TIB-71™      
          Designations:  RAW 264.7 
          Depositors:   WC Raschke 
          Biosafety Level: 2 
          Shipped:  frozen 
          Medium & Serum:  See Propagation 
          Growth Properties: adherent
          Organism: Mus musculus (mouse) 
          Morphology: monocyte/macrophage

           
          Source: Tissue: ascites
          Strain: BALB/c
          Disease: Abelson murine leukemia virus-induced tumor
          Cell Type: macrophage; Abelson murine leukemia virus transformed
          Cellular Products: lysozyme [1207] 
          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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location. 
           
          Applications: Biological response [92560]
          transfection host (Roche FuGENE® Transfection Reagents)
          Receptors: complement (C3) [1207]
          Antigen Expression: H-2d
          Age:  adult 
          Gender:  male 
          Comments: This line was established from a tumor induced by Abelson murine leukemia virus. They are negative for surface immunoglobulin (sIg-), Ia (Ia-) and Thy-1.2 (Thy-1.2)This line does not secrete detectable virus particles and is negative in the XC plaque formation assay. The cells will pinocytose neutral red and will phagocytose latex beads and zymosan. They are capable of antibody dependent lysis of sheep erythrocytes and tumor cell targets. LPS or PPD treatment for 2 days stimulates lysis of erythrocytes but not tumor cell targets.Data communicated in Feb. 2007 by Dr Janet W. Hartley, indicates the expression of infectious ecotropic MuLV closely related, if not identical, to the Moloney MuLV helper virus used in the original virus inoculum. The cells also express polytropic MuLV, unsurprisingly based on the mouse passage history of the virus stocks [ PubMed 18177500].
          Propagation:  ATCC complete growth medium: 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%.
          Atmosphere: air, 95%; carbon dioxide (CO2), 5%
          Temperature: 37.0°C
          Subculturing:  Protocol: Subcultures are prepared by scraping.
          For a 75 cm2 flask, remove all but 10 ml culture medium (adjust amount accordingly for other culture vessels). Dislodge cells from the flask substrate with a cell scraper; aspirate and add appropriate aliquots of the cell suspension into new culture vessels.
          Subc*tion Ratio: A subc*tion ratio of 1:3 to 1:6 is recommended
          Medium Renewal: Replace or add medium every 2 to 3 days.
          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 30-2002
          recommended serum:ATCC 30-2020
          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
          32443: Denlinger LC, et al. Regulation of inducible nitric oxide synthase expression by macrophage purinoreceptors and calcium. J. Biol. Chem. 271: 337-342, 1996. PubMed: 8550583
          32466: Hambleton J, et al. Activation of c-Jun N-terminal kinase in bacterial lipopolysaccharide-stimulated macrophages. Proc. Natl. Acad. Sci. USA 93: 2774-2778, 1996. PubMed: 8610116
          32553: Taylor GA, et al. Identification of anovel GTPase, the inducibly expresed GTPase, that accumulates in response to interferon gamma. J. Biol. Chem. 271: 20399-20405, 1996. PubMed: 8702776
          32901: Li YM, et al. Molecular identity and cellular distribution of advanced glycation endproduct receptors: relationship of p60 to OST-48 and p90 to 80K-H membrane proteins. Proc. Natl. Acad. Sci. USA 93: 11047-11052, 1996. PubMed: 8855306
          33046: Panneerselvam K, Freeze HH. Mannose enters mammalian cells using a specific transporter that is insensitive to glucose. J. Biol. Chem. 271: 9417-9421, 1996. PubMed: 8621609
          33076: Lokuta MA, et al. Mechanisms of murine RANTES chemokine gene induction by newcatle disease virus. J. Biol. Chem. 271: 13731-13738, 1996. PubMed: 8662857
          33162: Taylor MF, et al. In vitro efficacy of morpholino-modified antisense oligomers directed against tumor necrosis factor-alpha mRNA. J. Biol. Chem. 271: 17445-17452, 1996. PubMed: 8663413
          92560: Standard Practice for Testing for Biological Responses to Particles in Vitro. West Conshohocken, PA:ASTM International;ASTM Standard Test Method F 1903-98R03.
          16173094: Hartley JW, et al. Expression of infectious murine leukemia viruses by RAW264.7 cells, a potential complication for studies with a widely used mouse macrophage cell line. Retrovirology. 4: 5:1, 2008. PubMed 18177500.
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