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      NG108-15

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      產品名稱: NG108-15
      產品型號: HB-12317 NG108-15 小鼠神經細胞瘤與大鼠神經膠質瘤之融合細胞
      產品廠商: 美國標準生物品收藏中心(ATCC)
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      簡單介紹

      HB-12317 NG108-15 小鼠神經細胞瘤與大鼠神經膠質瘤之融合細胞,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!


      NG108-15 的詳細介紹
      HB-12317 NG108-15  小鼠神經細胞瘤與大鼠神經膠質瘤之融合細胞
      ATCC® Number: HB-12317?    Price:
      Designations: NG108-15 [108CC15]
      Depositors:  Univ. Texas Southwestern Medical Cntr.
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Mus musculus (neuroblastoma); Rattus norvegicus (glioma) (mouse (neuroblastoma); rat (glioma))
      Morphology: flat; round; 10 to 100 micrometers diameter
      HB-12317 NG108-15 小鼠神經細胞瘤與大鼠神經膠質瘤之融合細胞
      Source: Organ: brain
      Disease: glioblastoma; neuroblastoma
      Cell Type: somatic cell hybrid
      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.
       
      Applications: transfection host (Nucleofection technology from Lonza
      Roche FuGENE® Transfection Reagents)
      Comments: The NG108-15 cell line, originally named 108CC15, was developed in 1971 by Bernd Hamprecht. [112482]
      The line was formed by fusing mouse N18TG2 neuroblastoma cells with rat C6-BU-1 glioma cells in the presence of inactivated Sendai virus. [51493]
      Propagation: ATCC complete growth medium: The base medium for this cell line is Dulbecco's Modified Eagle's Medium without sodium pyruvate . To make the complete growth medium, add the following components to the base medium:
      • 0.1 mM hypoxanthine (final conc.)
      • 400 nM aminopterin (final conc.)
      • 0.016 mM thymidine (final conc.)
      • 10% fetal bovine serum (final conc.)
        Temperature: 37.0°C
      Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:6 to 1:10 is recommended
      Medium Renewal: Every 2 to 3 days
      Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 ml of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37C) until the cells detach.
      Add fresh culture medium, aspirate and dispense into new culture flasks.
      Preservation: Freeze medium: Complete growth medium, 92.5%; DMSO, 7.5%
      Storage temperature: liquid nitrogen vapor phase
      Related Products: recommended serum:ATCC 30-2020
      References: 51492: Hamprecht B. Structural, electrophysiological, biochemical, and pharmacological properties of neuroblastoma-glioma cell hybrids in cell culture. Int. Rev. Cytol. 49: 99-170, 1977. PubMed: 16829
      51493: Hamprecht B, et al. Culture and characteristics of hormone-responsive neuroblastoma X glioma hybrid cells. Methods Enzymol. 109: 316-341, 1985. PubMed: 2985920
      112482: Bernd Hamprecht, personal communication
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