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      產品名稱: U-118 MG 人腦星形膠質母細胞瘤
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      產品廠商: 美國標準生物品收藏中心(ATCC)
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      U-118 MG 人腦星形膠質母細胞瘤ATCC 細胞|細胞系|細胞株|腫瘤細胞|細胞|貼壁細胞|懸浮細胞|,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,


      U-118 MG 人腦星形膠質母細胞瘤 的詳細介紹

      U-118 MG 人腦星形膠質母細胞瘤
      U-118 MG (ATCC® HTB-15?)
      Organism  Homo sapiens, human 
      Tissue  brain
      Cell Type  Glioblastoma 
      Product Format  frozen 
      Morphology  mixed 
      Culture Properties  adherent 
      Biosafety Level  1 
      Disease  classified as grade IV as of 2007, glioblastoma; astrocytoma 
      Age  50 years 
      Gender  male 
      Ethnicity  Caucasian 
      Storage Conditions  liquid nitrogen vapor phase 
      tion  U-118 MG and U-138 MG are very similar cytogenetically and share at least six derivative marker chromosomes.
      This is one of a number of cell lines derived from malignant gliomas (see also ATCC HTB-14 and ATCC HTB-16) by J. Ponten and associates from 1966 to 1969.
      Clinical Data  50 years
      Caucasian
      male
      Antigen Expression  Blood Type A, Rh+; HLA Aw24, A28, B12, Bw47
      Tumorigenic  Yes 
      Effects  Yes, in nude mice inoculated subcutaneously with 10(7) cells
      (Tumors developed within 21 days at 100% frequency (5/5).)
      Comments  NOTE: The two glioblastoma cell lines, U-118 MG (HTB-15) and U-138 MG (HTB-16), reportedly from different individuals have identical VNTR and similar STR patterns.
      U-118 MG and U-138 MG are very similar cytogenetically and share at least six derivative marker chromosomes.
      Mycoplasma contamination was eliminated in 1987 by treatment with BM-Cycline over a six week culture period.

      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%.
       
      Subculturing  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 37°C) until the cells detach. Add fresh culture medium, aspirate and dispense into new culture flasks.
      Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended
      Medium Renewal: 2 to 3 times per week
      Cryopreservation  Freeze medium: Complete growth medium, 95%; DMSO, 5%
      Storage temperature: liquid nitrogen vapot temperature
      Culture Conditions  Temperature: 37°C

      STR Profile  Amelogenin: X,Y
      CSF1PO: 11,12
      D13S317: 9
      D16S539: 12,13
      D5S818: 11
      D7S820: 9
      THO1: 6
      TPOX: 8
      vWA: 18
      Isoenzymes  AK-1, 1-2
      ES-D, 1
      G6PD, B
      GLO-I, 1-2
      Me-2, 1
      PGM1, 2
      PGM3, 2

      Name of Depositor  J Ponten 
      Year of Origin  1966 
      References  Beckman G, et al. G-6-PD and PGM phenotypes of 16 continuous human tumor cell lines. Evidence against cross-contamination and contamination by HeLa cells. Hum. Hered. 21: 238-241, 1971. PubMed: 4332744

      Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871

      Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080

      Olopade OI, et al. Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas. Cancer Res. 52: 2523-2529, 1992. PubMed: 1568221

      Ponten J, Macintyre EH. Long term culture of normal and neoplastic human glia. Acta Pathol. Microbiol. Scand. 74: 465-486, 1968. PubMed: 4313504

      Pollack MS, et al. HLA-A, B, C and DR alloantigen expression on forty-six cultured human tumor cell lines. J. Natl. Cancer Inst. 66: 1003-1012, 1981. PubMed: 7017212

      Bluestein HG. Neurocytotoxic antibodies in serum of patients with systemic lupus erythematosus. Proc. Natl. Acad. Sci. USA 75: 3965-3969, 1978. PubMed: 279013

      Cairns P, et al. Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions. Cancer Res. 57: 5356-5359, 1997. PubMed: 9393760

      Tumors developed within 21 days at 100% frequency (5/5).
       

      References  Beckman G, et al. G-6-PD and PGM phenotypes of 16 continuous human tumor cell lines. Evidence against cross-contamination and contamination by HeLa cells. Hum. Hered. 21: 238-241, 1971. PubMed: 4332744

      Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871

      Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080

      Olopade OI, et al. Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas. Cancer Res. 52: 2523-2529, 1992. PubMed: 1568221

      Ponten J, Macintyre EH. Long term culture of normal and neoplastic human glia. Acta Pathol. Microbiol. Scand. 74: 465-486, 1968. PubMed: 4313504

      Pollack MS, et al. HLA-A, B, C and DR alloantigen expression on forty-six cultured human tumor cell lines. J. Natl. Cancer Inst. 66: 1003-1012, 1981. PubMed: 7017212

      Bluestein HG. Neurocytotoxic antibodies in serum of patients with systemic lupus erythematosus. Proc. Natl. Acad. Sci. USA 75: 3965-3969, 1978. PubMed: 279013

      Cairns P, et al. Genomic organization and mutation analysis of Hel-N1 in lung cancers with chromosome 9p21 deletions. Cancer Res. 57: 5356-5359, 1997. PubMed: 9393760

      Tumors developed within 21 days at frequency (5/5).
       

       

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