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      產品詳情
      • 產品名稱:NIHOVCAR-3 人卵巢癌細胞

      • 產品型號:HTB-161
      • 產品廠商:美國標準生物品收藏中心(ATCC)
      • 產品價格:0
      • 折扣價格:0
      • 產品文檔:
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      簡單介紹:
      HTB-161 NIH:OVCAR-3 人卵巢癌細胞,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!
      詳情介紹:
      HTB-161 NIH:OVCAR-3 人卵巢癌細胞
      ATCC® Number: HTB-161?    Price: $272.00
      Designations: NIH:OVCAR-3
      Depositors:  R Ozols, TC Hamilton
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Homo sapiens (human)
      Morphology: epithelial
      HTB-161 NIH:OVCAR-3 人卵巢癌細胞
      Source: Organ: ovary
      Disease: adenocarcinoma
      Cell Type: epithelial
      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: 1982
      Applications: transfection host (Roche FuGENE® Transfection Reagents)
      Receptors: androgen receptor, positive; estrogen receptor, positive; progesterone receptor, positive
      Tumorigenic: Yes
      DNA Profile (STR): Amelogenin: X
      CSF1PO: 11,12
      D13S317: 12
      D16S539: 12
      D5S818: 11,12
      D7S820: 10
      THO1: 9,9.3
      TPOX: 8
      vWA: 17
      Cytogenetic Analysis: The cell line is aneuploid human female, with chromosome counts in the sub to near-triploid range. Several normal chromosomes (N11, N13, N14, N15, N16, N17, and N22) are clearly under-represented. Many of these missing chromosomes are represented in the large number of cytogenetically altered chromosomes identified as marker chromosomes. In addition to the marker chromosomes, there are a large number of other structurally abnormal and unassignable chromosomes that are not recognized as markers. Random loss and gain of chromosomes from cell to cell are noted in the exact chromosome counts and in the analysis of the karyotypes.
      Isoenzymes: AK-1, 1
      ES-D, 1
      G6PD, B
      GLO-I, 1
      PGM1, 1
      PGM3, 1
      Age: 60 years
      Gender: female
      Ethnicity: Caucasian
      Comments: The NIH:OVCAR-3 line was established in 1982 by T.C. Hamilton, et al. from the malignant ascites of a patient with progressive adenocarcinoma of the ovary.
      Forms colonies in soft agar and has an abnormal karyotype.
      Resistant to clinically relevant concentrations of adriamycin, melphalan and cisplatin.
      Both cultured cells and xenografts exhibit androgen and estrogen receptors.
      Xenograft models have been used to show that treatment with 17 beta estradiol can induce progesterone receptors in this human ovarian carcinoma.
      NIH:OVCAR-3 is an appropriate model system in which to study drug resistance in ovarian cancer, and the presence of hormone receptors should be useful for the evaluation of hormonal therapy.
      Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: 0.01 mg/ml bovine insulin; fetal bovine serum to a final concentration of 20%.
      Temperature: 37.0°C
      Atmosphere: air, 95%; carbon dioxide (CO2), 5%
      Subculturing: Protocol: Remove medium, and rinse with 0.25% trypsin, 0.53 mM 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.
      Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
      Medium Renewal: Every 2 to 3 days
      Preservation: Freeze medium: Complete growth medium, 95%; DMSO, 5%
      Storage temperature: liquid nitrogen vapor temperature
      Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001
      recommended serum:ATCC 30-2020
      References: 1127: Hamilton TC, et al. Characterization of a human ovarian carcinoma cell line (NIH:OVCAR-3) with androgen and estrogen receptors. Cancer Res. 43: 5379-5389, 1983. PubMed: 6604576
      1128: Hamilton TC, et al. Induction of progesterone receptor with 17beta-estradiol in human ovarian cancer. J. Clin. Endocrinol. Metab. 59: 561-563, 1984. PubMed: 6746867
      22949: Rogan AM, et al. Reversal of adriamycin resistance by verapamil in human ovarian cancer. Science 224: 994-996, 1984. PubMed: 6372095
      23051: Hamilton TC, et al. Characterization of a xenograft model of human ovarian carcinoma which produces ascites and intraabdominal carcinomatosis in mice. Cancer Res. 44: 5286-5290, 1984. PubMed: 6333272
      23052: Green JA, et al. Potentiation of melphalan cytotoxicity in human ovarian cancer cell lines by glutathione depletion. Cancer Res. 44: 5427-5431, 1984. PubMed: 6488194
      23100: Caffrey PB, Frenkel GD. Selenite cytotoxicity in drug resistant and nonresistant human ovarian tumor cells. Cancer Res. 52: 4812-4816, 1992. PubMed: 1511444
      23164: Hamilton TC, et al. Experimental model systems of ovarian cancer: applications to the design and evaluation of new treatment approaches. Semin. Oncol. 11: 285-298, 1984. PubMed: 6385258
      23329: Godwin AK, et al. High resistance to cisplatin in human ovarian cancer cell lines is associated with marked increase of glutathione synthesis. Proc. Natl. Acad. Sci. USA 89: 3070-3074, 1992. PubMed: 1348364
      32582: Chang K, Pastan I. Molecular cloning of mesothelin, a differentiation antigen present on mesothelium, mesotheliomas, and ovarian cancers. Proc. Natl. Acad. Sci. USA 93: 136-140, 1996. PubMed: 8552591
      32690: Omelyanenko V, et al. HPMA copolymer-anticancer drug-OV-TL16 antibody conjugates. II. Processing in epithelial ovarian carcinoma cells in vitro. Int. J. Cancer 75: 600-608, 1998. PubMed: 9466663
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