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      Calu-6 人肺癌細(xì)胞系(未分化癌)

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      產(chǎn)品名稱: Calu-6 人肺癌細(xì)胞系(未分化癌)
      產(chǎn)品型號: HTB-56
      產(chǎn)品廠商: 美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      產(chǎn)品文檔: 無相關(guān)文檔


      簡單介紹

      HTB-56 Calu-6 人肺癌細(xì)胞系(未分化癌)原代細(xì)胞|細(xì)胞系|細(xì)胞株|菌種;細(xì)胞庫管理規(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!


      Calu-6 人肺癌細(xì)胞系(未分化癌) 的詳細(xì)介紹
      HTB-56 Calu-6 人肺癌細(xì)胞系(未分化癌)
      ATCC® Number: HTB-56?    Price: $329.00
      Designations: Calu-6
      Depositors:  J Fogh
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Homo sapiens (human)
      Morphology: epithelial

      Source: Organ: unknown, probably lung
      Disease: anaplastic carcinoma
      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.
      Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
      Atmosphere: air, 95%; carbon dioxide (CO2), 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 which 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 37C 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 37C.

      Interval: every 6 to 8 days
      Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended
      Medium Renewal: 2 to 3 times per week
      Preservation: Freeze medium: Culture medium, 95%; DMSO, 5%
      Storage temperature: liquid nitrogen vapor phase

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