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      當前位置:首頁 >產(chǎn)品中心>細胞庫>小鼠正常細胞>CCL-9.1NCTC 1469 小鼠正常肝細胞

      NCTC 1469 小鼠正常肝細胞

      簡要描述:CCL-9.1 NCTC 1469 小鼠正常肝細胞,原代細胞|細胞系|細胞株|菌種;細胞庫管理規(guī)范,
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      • 產(chǎn)品型號:CCL-9.1
      • 廠商性質:生產(chǎn)廠家
      • 更新時間:2025-11-12
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      CCL-9.1 NCTC 1469 小鼠正常肝細胞 的詳細介紹

      CCL-9.1 NCTC 1469 小鼠正常肝細胞

      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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