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      TOV-21G 人卵巢癌細胞

      更新時間:2016-08-01      點擊次數:3415
      Designations:TOV-21G
      Depositors: University of Montreal
      Biosafety Level:1
      Shipped:frozen
      Medium & Serum:See Propagation
      Growth Properties:adherent
      Organism:Homo sapiens deposited as human
      Morphology:epithelial
       
      Source:Organ: ovary 
      Tumor Stage: grade 3, stage III 
      Disease: primary malignant adenocarcinoma; clear cell carcinoma
      Cellular Products:keratin
      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.
      Applications:Like OV-90 (ATCC CRL-11732 ), the OV-21G (ATCC CRL-11730 ) cell line exhibits a deletion at chromosome 3p24. The TOV-112D (ATCC CRL-11731 ) cell line does not exhibit a deletion at chromosome 3p24.
      Tumorigenic:Yes
      Oncogene:p53 + (wild type)
      DNA Profile (STR):Amelogenin: X 
      CSF1PO: 13,15 
      D13S317: 11,12 
      D16S539: 10,12 
      D5S818: 12,13 
      D7S820: 12 
      THO1: 7,9.3 
      TPOX: 8,11 
      vWA: 17
      Cytogenetic Analysis:47, XX, +10 [49408 ]
      Age:62 years
      Gender:female
      Comments:This cell line was initiated in October of 1991 from a patient of French-Canadian descent with no family history of ovarian cancer. 
      Like OV-90 (ATCC CRL-11732 ), the OV-21G (ATCC CRL-11730 ) cell line exhibits a deletion at chromosome 3p24. The TOV-112D (ATCC CRL-11731 ) cell line does not exhibit a deletion at chromosome 3p24.
      Propagation:ATCC complete growth medium: The base medium for this cell line is a 1:1 mixture of MCDB 105 medium containing a final concentration of 1.5 g/L sodium bicarbonate and Medium 199 containing a final concentration of 2.2 g/L sodium bicarbonate. To make the complete growth medium, add the following components to the base medium:
      • fetal bovine serum to a final concentration of 15%

      • 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 0.05% (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.

      Subc*tion Ratio: A subc*tion ratio of 1:3 to 1:4 is recommended 
      Medium Renewal: Every 3 to 4 days
      Preservation:Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO 
      Storage temperature: liquid nitrogen vapor phase
      Related Products:recommended serum:ATCC 30-2020
      References:

      42090: Mes-Masson AM, Provencher D. Primary cultures of normal and tumoral human ovarian epithelium. US Patent 5,710,038 dated Jan 20 1998
      49408: Provencher DM, et al. Characterization of four novel epithelial cancer cell lines. In Vitro Cell. Dev. Biol. Anim. 36: 357-361, 2000. PubMed: 10949993

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