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A101D

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  • 2026年01月08日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 库存

      大量

    • 细胞形态

      上皮样

    • 物种来源

    • 是否是肿瘤细胞

      1

    • 器官来源

      皮肤

    • 生长状态

      贴壁生长

    • 运输方式

      冻存运输

    • 相关疾病

      黑色素瘤

    • ATCC Number

      CRL-7898™

    • 年限

      56 years

    Designations: A101D
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Homo sapiens
    Morphology: epithelial

    Source: Organ: skin
    Disease: melanoma
    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.
    DNA Profile (STR): Amelogenin: X
    CSF1PO: 11
    D13S317: 11,12
    D16S539: 12
    D5S818: 12
    D7S820: 10
    THO1: 8,9.3
    TPOX: 8,11
    vWA: 16,18
    Cytogenetic Analysis: modal number = 63; range = 48 to 82
    Isoenzymes: ADA, 1
    ES-D, 1
    G6PD, B
    PEP-D, 1
    PGD, A
    PGM1, 1-2
    PGM3, 1
    Age: 56 years
    Gender: male
    Ethnicity: Caucasian
    Comments: Part of the NBL Cell Line Collection. This cell line is neither produced nor fully characterized by ATCC . We do not guarantee that it will maintain a specific morphology, purity, or any other property upon passage.
    Please see the NBL Repository description. ATCC HTB-140 (Hs 294T) and ATCC CRL-7898 (A101D) were isolated from the same donor tissue
    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%.
    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 0.25% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which contains a 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 37C 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 37C.

    Subcultivation Ratio: A ratio of 1:4 is recommended
    Medium Renewal: Every 2 to 3 days
    Preservation: Freeze medium: culture medium, 95%; DMSO, 5%
    Storage temperature: liquid nitrogen vapor phase
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2002
    recommended serum:ATCC 30-2020
    0.25% (w/v) Trypsin - 0.53 mM EDTA in Hank' BSS (w/o Ca++, Mg++):ATCC 30-2101
    References: 23218: Giard DJ, et al. In vitro cultivation of human tumors: establishment of cell lines derived from a series of solid tumors. J. Natl. Cancer Inst. 51: 1417-1423, 1973. PubMed: 4357758

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    图标文献和实验
    相关实验
    • DD-loop

      指DNA双链的局部,由具有互补性单链 DNA与之结合所产生的环状结构。当 DNA复制开始,在原来的双链中仅一方被新合成的短 DNA单链被置换的情况下可以见到(为 Displacement loop之简称)。可通过人工使 DNA单链结合来制成此结构。由 RNA单链所产生的类似结构称为 R环。  

    • 2D Gel Electrophoresis(图)

      of each component.2D gel electrophoresis is generally used as a component of proteomics and is the step used for the isolation of proteins for further characterisation by mass spectroscopy. In the lab this technique is used for 2 main purposes, firstly for the large

    • 2D Gel Electrophoresis

      of each component. 2D gel electrophoresis is generally used as a component of proteomics and is the step used for the isolation of proteins for further characterisation by mass spectroscopy. In the lab this technique is used for 2 main purposes, firstly

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