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    當前位置:首頁 >產品中心>細胞庫>小鼠腫瘤細胞、癌細胞>CRL-6475B16-F10 小鼠黑色素瘤細胞株

    B16-F10 小鼠黑色素瘤細胞株

    簡要描述:CRL-6475 B16F10 小鼠黑色素瘤高轉移細胞,原代細胞|細胞系|細胞株|菌種;細胞庫管理規范,提供的細胞株背景清楚,提供參考文獻和培養條件!

    • 產品型號:CRL-6475
    • 廠商性質:生產廠家
    • 更新時間:2025-06-28
    • 訪  問  量:2353

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    詳細介紹

    產品名稱--小鼠黑色素瘤細胞;B16-F10(種屬鑒定) 

    英文名--B16-F10 

    規格--1×10?cells/T25培養瓶 

    培養--RPMI1640+10%FBS 

    別稱--B16-F10;B16/F10; B16 F10; B16F10; B16 melanoma F10 

    生長特性--貼壁生長 

    培養基--B16-F10完培養基 

    培養條件--氣相:空氣,95%;CO2,5%溫度:37℃ 

    傳代方法--消化3-5分鐘。1:2。3天內可長滿。 

    特征特性--B16-F10是B16-F0的亞系。 


    ATCC® Number:CRL-6475™  Price:$269.00
    Designations:B16-F10

    Biosafety Level:1

    Shipped:frozen

    Medium & Serum:See Propagation

    Growth Properties:adherent

    Organism:Mus musculus (mouse)

    Morphology:melanocyte
    B16-F10  小鼠黑色素瘤細胞株


    Source:Organ: skin
    Strain: C57BL/6J
    Disease: melanoma


    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.
    CRL-6475

    Applications:transfection host (technology from amaxa)

    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%.
    Temperature: 37.0°C
    Atmosphere: air, 95%; carbon dioxide (CO2), 5%


    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.


      1. Subc*tion Ratio: A subc*tion ratio of 1:10 is recommended
        Medium Renewal: Every 2 to 3 days



    Preservation:Freeze medium: culture medium, 95%; DMSO, 5%
    Storage temperature: liquid nitrogen vapor phase



    CRL-6475

















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