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      大鼠肝癌細(xì)胞系

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      產(chǎn)品名稱: 大鼠肝癌細(xì)胞系
      產(chǎn)品型號(hào): CRL-1600
      產(chǎn)品廠商: 美國(guó)標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      產(chǎn)品文檔: 無(wú)相關(guān)文檔


      簡(jiǎn)單介紹

      CRL-1600 H4-ⅡE 大鼠肝癌細(xì)胞系,原代細(xì)胞、細(xì)胞系。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Z優(yōu)培養(yǎng)條件,


      大鼠肝癌細(xì)胞系 的詳細(xì)介紹
      CRL-1600 H4-ⅡE 大鼠肝癌細(xì)胞系
      ATCC® Number: CRL-1600?    Price: $355.00
      Designations: H4-II-E-C3
      Depositors:  JE Becker
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Rattus norvegicus (rat)
      Morphology: epithelial

      Source: Organ: liver
      Strain: AxC
      Disease: hepatoma
      Cellular Products: tyrosine aminotransferase; albumin; transferrin; prothrombin
      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.
       
      Tumorigenic: Yes
      Gender: male
      Comments: Tyrosine amino transferase is inducible with glucorticoids, insulin or cAMP derivatives.
      The cells are productively infected with a retrovirus.
      Propagation: ATCC complete growth medium: Dulbecco's modified Eagle's medium with 4 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate and 4.5 g/L glucose, 75%; horse serum, 20%; fetal bovine serum, 5%.
      Temperature: 37.0°C
      Subculturing: Protocol:
      1. Remove and discard culture medium.
      2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor.
      3. Add 2.0 to 3.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
        Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
      4. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
      5. Add appropriate aliquots of the cell suspension to new culture vessels.
      6. Incubate cultures at 37°C.

          Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:12 is recommended
          Medium Renewal: 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
      recommended serum:ATCC 30-2040
      References: 1084: Potter VR, Morse PA Jr.. Pyrimidine metabolism in tissue culture cells derived from rat hepatomas. I. Suspension cell cultures derived from the Novikoff hepatoma. Cancer Res. 25: 499-508, 1965. PubMed: 14297488
      1217: Reuber MD. A transplantable bile-secreting hepatocellular carcinoma in the rat. J. Natl. Cancer Inst. 26: 891-899, 1961. PubMed: 13740982
      26102: Weinstein IB, et al. Type C virus from cell cultures of chemically induced rat hepatomas. Science 178: 1098-1100, 1972. PubMed: 4343844
      33030: Klemm DJ, et al. Adenovirus E1A proteins regulate phosphoenolpyruvate carboxykinase gene transcription through multiple mechanisms. J. Biol. Chem. 271: 8082-8088, 1996. PubMed: 8626493
      58076: Peraino C, et al. Hepatomas in tissue culture compared with adapting liver in vivo. Natl. Cancer Inst. Monogr. 13: 229-245, 1964. PubMed: 14143233
       
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