HCC38

HCC38

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  • 2025年08月16日
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    • 详细信息
    • 技术资料
    • 库存

      大量

    • 器官来源

      乳房

    • 运输方式

      冻存运输

    • 生长状态

      贴壁生长

    • 物种来源

    • 是否是肿瘤细胞

      1

    • 细胞形态

      上皮样

    • 组织来源

      duct

    • 年限

      TNM stage IIB, grade 3

    • 相关疾病

      导管癌

    • ATCC Number

      CRL-2314™

    Designations: HCC38
    Depositors:  AF Gazdar, AK Virmani
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent, single cells and loosely attached clusters
    Organism: Homo sapiens
    Morphology: epithelial

    Source: Organ: mammary gland; breast
    Tissue: duct
    Tumor Stage: TNM stage IIB, grade 3
    Disease: primary ductal carcinoma
    Cellular Products: Epithelial glycoprotein 2 [EGP2]; cytokeratin 19
    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.
    Restrictions: The line is available with the following restrictions: 1. This cell line was deposited at the ATCC by Dr. Adi F. Gazdar and is provided for research purposes only. Neither the cell line nor products derived from it may be sold or used for commercial purposes. Nor can the cells be distributed to third parties for purposes of sale, or producing for sale, cells or their products. The cells are provided as service to the research community. They are provided without warranty of merchantability or fitness for a particular purpose or any other warranty, expressed or implied. 2. Any proposed commercial use of the these cells, or their products must first be negotiated with the University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd., Dallas, Texas 75235. Telephone (214) 648-1888, Email TechnologyDevelopment@UTSouthwestern.edu, or Fax: (214) 951-0935.
    Isolation: Isolation date: April 27, 1992
    Applications: HCC38 is positive for the epithelial cell specific marker Epithelial Glycoprotein 2 [EGP2] and for cytokeratin 19, and is negative for expression of estrogen receptor (ER) and progesterone receptor (PR).

    The cells are negative for expression of Her2-neu but positive for expression of p53
    Receptors: estrogen receptor, not expressed
    progesterone receptor, not expressed
    Oncogene: her2/neu -; p53 +
    DNA Profile (STR): Amelogenin: X
    CSF1PO: 12
    D13S317: 12,14
    D16S539: 10,14
    D5S818: 9
    D7S820: 10
    THO1: 9.3
    TPOX: 9,12
    vWA: 16,17
    Cytogenetic Analysis: Number of cells examined = 59; Modal Chromosome Number = 75 with a range of 65 to 79; Polyploidy Rate = 22%
    Age: 50 years adult
    Gender: female
    Ethnicity: Caucasian, White
    Comments: The cells are negative for expression of Her2-neu but positive for expression of p53
    This cell line was initiated on 4/27/92 and took 32 months to establish.
    HCC38 was initiated from a 50-year-old white female with a prior history of leiomyosarcoma; her mother died of breast cancer.
    The tumor was classified as TMN Stage IIB, Grade 3, with 3/28 lymph node metastasis.
    HCC38 is positive for the epithelial cell specific marker Epithelial Glycoprotein 2 [EGP2] and for cytokeratin 19, and is negative for expression of estrogen receptor (ER) and progesterone receptor (PR).
    HCC38 contains a homozygous deletion at 3p12.
    Cytogenetics: Derivatives and Markers
    At least 45 distinct derivative chromosomes were detected in most metaphases, including two large metacentric markers which are approximately 1.5 times longer than a normal A group chromosome.
    Other derivative chromosomes: del(1)(q24); del(1)(p22); del(1)(p13); add(1)(p12); del(2)(p16); add(3)(q10); del(3)(q13); ?del(4)(q13) (two copies per cell); del(5)?(q23q33); der (7)(pter�q11::?hsr); del(7)(p?);
    del(9)(p12); add(9)(p10); ?der(11); add(12)(q24)(very long); add(14)(p11); add(17)(p12); der(18); der(X); plus approx. 17-24 markers of unknown origin per cell.
    Cytogenetics: Comments
    This is a hyper-triploid human cell line with a modal chromosome number of 75.
    Homogeneously staining regions and dicentric chromosomes were observed. Every chromosome pair had a least one rearrangement; however, normal copies of chromosomes 2, 6, 11, 13, 16 and 20 were consistently seen.
    No normal X chromosomes were observed and Y chromosomes were absent by QM staining.
    The following structural rearrangements were observed in 30 metaphases: an acentric fragment in 2/30 metaphases, a minute in 3/30, a chromosome break in 3/30, a chromatid break in 5/30, a ring chromosome in 1/30, and double minutes in 11/30 (1-5 copies).
    Pulverized chromosomes were reported in 5% of metaphases. C-banding revealed that several of the large markers are dicentric. No normal X chromosomes were observed and Y chromosomes were absent by QM staining.
    Normal copies of chromosomes 2,6,11,13,16 and 20 were seen.
    Composite karyotype: 65-79<3n> der(X), -1,-1,-1, del(1)(q24), del(1)(p22),del(1)(p13),add(1)(p12),-2,del(2)(p16)x2,-3,-3,-3, ?add(3)(q10),del(3)(q13)x2,-4,-4,-4, ?del(4)(q13)x2,-5, -5,-5,del(5)?(q23q33)x2,-6,-6,-7,-7,-7,
    der (7)(pter�q11::?hsr), del(7)(p?)x2,-8,-8,-8,-9,-9,-9,del(9)(p12)x2,add(9)(p10)x2, -10,-10,-10,-11,?der(11),-12,-12,-12, add(12)(q24), -13,-13,-14,-14,-14,
    add(14)(p11)x2,-15,-15,-15,-17,-17,-17, add(17)(p12)x2,-18,-18,-18,der(18),-19,-19,-19,-21,-21, -22,-22,+17 to 24 mar[cp11].
    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: fetal bovine serum to a final concentration of 10%.
    Temperature: 37.0°C
    Atmosphere: air, 95%; carbon dioxide (CO2), 5%
    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 that contains 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 37�C 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 37�C.

        Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
        Medium Renewal: Every 3 to 5 days
    Preservation: Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
    Storage temperature: liquid nitrogen vapor phase
    Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001
    recommended serum:ATCC 30-2020
    EBV-transformed cell line from the same patient:ATCC CRL-2346
    purified DNA:ATCC CRL-2314D
    purified RNA:ATCC CRL-2314R
    References: 38266: Gazdar AF, et al. Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer. Int. J. Cancer 78: 766-774, 1998. PubMed: 9833771
    38330: Sundarsan V, et al. Homozygous deletions at 3p12 in breast and lung cancer. Oncogene 17: 1723-1729, 1998. PubMed: 9796701

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