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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)> CCL-9.1 NCTC 1469 小鼠正常肝細(xì)胞

          [供應(yīng)]CCL-9.1 NCTC 1469 小鼠正常肝細(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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          CCL-9.1 NCTC 1469 小鼠正常肝細(xì)胞,原代細(xì)胞|細(xì)胞系|細(xì)胞株|菌種;細(xì)胞庫(kù)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
          CCL-9.1 NCTC 1469 小鼠正常肝細(xì)胞 的詳細(xì)介紹
          CCL-9.1 NCTC 1469 小鼠正常肝細(xì)胞
          ATCC® Number: CCL-9.1™    Price: $329.00
          Designations: NCTC clone 1469 [derivative of NCTC 721]
          Depositors:  VJ Evans
          Biosafety Level: 1
          Shipped: frozen
          Medium & Serum: See Propagation
          Growth Properties: adherent
          Organism: Mus musculus (mouse)
          Morphology: epithelial

          Source: Organ: liver
          Strain: C3H/An
          Disease: normal
          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.
           
          Isolation: Isolation date: April, 1952
          Virus Susceptibility: Vesicular stomatitis virus
          Human poliovirus 1
          Antigen Expression: H-2k
          Cytogenetic Analysis: modal number = 41; range = 38 to 86.
          Two marker chromosomes present: One metacentric with one pair of arms having achromatic gaps near centromere; and an acrocentric with salites.
          Age: newborn
          Gender: male
          Comments: Tested and found negative for ectromelia virus (mousepox).
          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: horse 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. Remove old medium, add fresh medium and dislodge the cells from the floor of the flask. Aspirate cells and dispense the suspension into new flasks.
          A standard trypsinizaton may be used if desired.
          The culture medium in heavy cultures may be turbid in appearance and and give the gross impression of bacterial contamination.
          It is characteristic of this line to shed viable cells into the medium, thus rendering the medium turbid. The shed cells are viable and may be used to initiate new cultures.
          Subc*tion Ratio: A subc*tion ratio of 1:2 to 1:4 is recommended
          Medium Renewal: 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 30-2002
          recommended serum:ATCC 30-2040
          References: 22167: Hobbs GL, et al. Establishment of a clone of mouse liver cells from a single isolated cell. J. Natl. Cancer Inst. 18: 701-707, 1957. PubMed: 13502690
          26070: Evans VJ, et al. The growth in vitro of massive cultures of liver cells. J. Natl. Cancer Inst. 12: 1245-1265, 1952. PubMed: 14939026
          26074: . . J. Natl. Cancer Inst. 23: 823, 1959.
          26076: . . J. Natl. Cancer Inst. 27: 29, 1961.
          26078: Evans VJ, et al. Studies on culture lines derived from mouse liver parenchymatous cells grown in long-term tissue culture. Cancer Res. 12: 261-266, 1958. PubMed: 13523589
          26079: . . Fed. Proc. 17: 967, 1958.
          26081: Westfall BB. Characterization of cells in tissue culture. Natl. Cancer Inst. Monogr. 7: 147-158, 1962. PubMed: 14006338

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