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H1HeLa

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  • 2026年06月28日
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    • 相关疾病

      腺癌

    • ATCC Number

      CRL-1958™

    • 年限

      31 years

    • 细胞形态

      上皮样

    • 运输方式

      冻存运输

    • 器官来源

      宫颈

    • 库存

      大量

    • 物种来源

    • 是否是肿瘤细胞

      0

    • 生长状态

      贴壁生长

    Designations: H1HeLa
    Depositors:  RR Rueckert
    Biosafety Level: 2 [Cells contain human papilloma virus (HPV-18) ]
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Homo sapiens
    Morphology: epithelial

    Source: Organ: cervix
    Disease: adenocarcinoma
    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.
    Reverse Transcript: negative
    DNA Profile (STR): Amelogenin: X
    CSF1PO: 9,10
    D13S317: 12,13.3
    D16S539: 9,10
    D5S818: 11,12
    D7S820: 8,12
    THO1: 7
    TPOX: 8,12
    vWA: 16,18
    Isoenzymes: G6PD, A
    Age: 31 years
    Gender: female
    Ethnicity: Black
    HeLa Markers: Y
    Comments: The H-Hela cell line was established by V. Hamparian from the HeLa cell line isolated by Gey, et al. (see ATCC CCL-2 ).
    This subline is susceptible to rhinoviruses and is useful for passaging and titrating rhinoviruses.
    The line is usually carried as monolayer cultures in Leibovitz's L-15 medium, but can be readily adapted to other media and to suspension culture (in media without Ca++).
    The H-HeLa line was cured of a mycoplasma contamination by W.M. Lee in Rueckert's laboratory and the cured line was given the designation H1-HeLa.
    Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Leibovitz's L-15 Medium, Catalog No. 30-2008. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
    Atmosphere: air, 100%
    Subculturing: Subcultivation Ratio: A subcultivation ratio of 1:4 to 1:10 is recommended
    Medium Renewal: 2 to 3 times per week
    Remove the medium and add fresh 0.25% trypsin, 0.03% EDTA solution, rinse and remove trypsin. Allow the culture to sit for 5 minutes at room temperature. Add fresh culture medium, aspirate and dispense into new flasks.
    References: 21853: Lee WM Ph.D. thesis, Univ. Wisconsin, 1991
    22695: Medappa KC, et al. On the structure of rhinovirus 1A. Virology 44: 259-270, 1971. PubMed: 4327717

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    图标文献和实验
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    • Preparation of HeLa Nuclear Extracts

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