Channel Catfish Ovary [CCO]

Channel Catfish Ovary [CCO]

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  • 2025年12月10日
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    • 详细信息
    • 技术资料
    • 细胞形态

      成纤维样

    • 生长状态

      贴壁生长

    • 运输方式

      冻存运输

    • 库存

      大量

    • 物种来源

      其他

    • 是否是肿瘤细胞

      0

    • 器官来源

      卵巢

    • 细胞类型

      成纤维细胞

    • ATCC Number

      CRL-2772™

    • 年限

      juvenile

    Designations: Channel Catfish Ovary [CCO]
    Depositors:  L Hanson
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Ictalurus punctatus
    Morphology: fibroblast

    Source: Organ: ovary
    Cell Type: fibroblast
    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: October, 1975
    Age: juvenile
    Comments: The CCO cell line was derived from the ovaries of a healthy, juvenile channel catfish in October 1975 (PubMed: 7390534]. CCO is the cell line of choice for the propagation and diagnosis of Channel Catfish Virus (CCV). It is the standard for diagnosing Channel Catfish Virus Disease (CCVD) in farm reared Channel Catfish. The cells were cured of mycoplasma contamination in 1989 using Ciprofloxacin [J. Aquat. Anim. Health 6: 82-84, 1994].
    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: fetal bovine serum to a final concentration of 10%.
    Atmosphere: air, 95%; carbon dioxide (CO2), 5%
    Temperature: 30.0°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 30�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 30�C.

    Subcultivation Ratio: 1:4 to 1:6 weekly
    Medium Renewal: Two to three times weekly
    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
    References: 61176: Bowser PR, Plumb JA. Channel catfish virus: comparative replication and sensitivity of cell lines from channel catfish ovary and the brown bullhead. J. Wildl. Dis. 16: 451-454, 1980. PubMed: 7411751
    61177: Bowser PR, Plumb JA. Fish cell lines: establishment of a line from ovaries of channel catfish. In Vitro 16: 365-368, 1980. PubMed: 7390534
    70166: Hanson LA, Thune RL. Ciprofloxacin treatment eliminates Mycoplasma in contaminated channel catfish ovary cells. J. Aquat. Anim. Health 6: 82-84, 1994.

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