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      • 產(chǎn)品名稱(chēng):CCL-9.1 NCTC 1469 小鼠正常肝細(xì)胞

      • 產(chǎn)品型號(hào):CCL-9.1
      • 產(chǎn)品廠商:美國(guó)標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      • 產(chǎn)品價(jià)格:0
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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!
      詳情介紹:
      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 ultimately 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 satellites.
      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.
      Subcultivation Ratio: A subcultivation 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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