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        當(dāng)前位置:首頁 >產(chǎn)品中心>細(xì)胞庫>小鼠正常細(xì)胞>CCL-9.1NCTC 1469 小鼠正常肝細(xì)胞

        NCTC 1469 小鼠正常肝細(xì)胞

        簡(jiǎn)要描述: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)胞庫管理規(guī)范,
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        • 產(chǎn)品型號(hào):CCL-9.1
        • 廠商性質(zhì):生產(chǎn)廠家
        • 更新時(shí)間:2025-05-24
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        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.
        CCL-9.1

        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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