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TOV-21G 人卵巢癌细胞

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 ultimately 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.

    Subcultivation Ratio: A subcultivation 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

    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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    CTLA4 Ig-24 中国仓鼠卵巢细胞 TOV-21G 人卵巢癌
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    CHO/dhFr- 仓鼠卵巢细胞,二氢叶酸还原酶缺陷 SK-OV-3 人卵巢癌细胞TOV-21G 人卵巢癌细胞TOV-21G 人卵巢癌细胞

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