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U-118 MG

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  • 2025年08月27日
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    • 是否是肿瘤细胞

      1

    • 相关疾病

      其他疾病

    • ATCC Number

      HTB-15™

    • 细胞形态

      混合型

    • 年限

      classified as grade IV as of 2007

    • 生长状态

      贴壁生长

    • 运输方式

      冻存运输

    • 器官来源

      大脑

    • 库存

      大量

    Designations: U-118 MG
    Depositors:  J Ponten
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Homo sapiens
    Morphology: mixed

    Source: Organ: brain
    Tumor Stage: classified as grade IV as of 2007
    Disease: glioblastoma; astrocytoma
    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.
    Tumorigenic: Yes
    Antigen Expression: Blood Type A, Rh+; HLA Aw24, A28, B12, Bw47
    DNA Profile (STR): 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
    Age: 50 years
    Gender: male
    Ethnicity: Caucasian
    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.
    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.
    Mycoplasma contamination was eliminated in 1987 by treatment with BM-Cycline over a six week culture period.
    Propagation: ATCC 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%.
    Temperature: 37.0°C
    Subculturing: Protocol: 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.
    Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:8 is recommended
    Medium Renewal: 2 to 3 times per week
    Preservation: Freeze medium: Complete growth medium, 95%; DMSO, 5%
    Storage temperature: liquid nitrogen vapot temperature
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002
    recommended serum:ATCC 30-2020
    References: 22159: 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
    22536: 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
    22539: 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
    23094: 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
    23128: Ponten J, Macintyre EH. Long term culture of normal and neoplastic human glia. Acta Pathol. Microbiol. Scand. 74: 465-486, 1968. PubMed: 4313504
    23226: 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
    23260: Bluestein HG. Neurocytotoxic antibodies in serum of patients with systemic lupus erythematosus. Proc. Natl. Acad. Sci. USA 75: 3965-3969, 1978. PubMed: 279013
    32276: 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

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      佚名     u检验(亦称T检验),它根据正态分布规律作假设检验(显著性检验)。当样本含量增大时,样本均数的分布趋向正态,这可看图6.1,t分布曲线以ν=9的一条比ν=3的更近似正态分布,再看附表3,表最下一行ν为∞时的t分布即是正态分布。故u检验用于大样本。   在仅有一条的标准正态曲线上,以u=1.96与-1.96为界,从此处向外的尾部面积共占

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      佚名     u检验(亦称T检验),它根据正态分布规律作假设检验(显著性检验)。当样本含量增大时,样本均数的分布趋向正态,这可看图6.1,t分布曲线以ν=9的一条比ν=3的更近似正态分布,再看附表3,表最下一行ν为∞时的t分布即是正态分布。故u检验用于大样本。   在仅有一条的标准正态曲线上,以u=1.96与-1.96为界,从此处向外的尾部面积共占

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