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LS 174T

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  • 2026年01月11日
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    • 年限

      Dukes' type B

    • 物种来源

    • 是否是肿瘤细胞

      1

    • 器官来源

      结肠

    • 库存

      大量

    • 运输方式

      冻存运输

    • 生长状态

      贴壁生长

    • 相关疾病

      大肠癌

    • ATCC Number

      CL-188™

    • 细胞形态

      上皮样

    Designations: LS 174T
    Depositors:  Northwestern University
    Biosafety Level: 1
    Shipped: frozen
    Medium & Serum: See Propagation
    Growth Properties: adherent
    Organism: Homo sapiens
    Morphology: epithelial

    Source: Organ: colon
    Tumor Stage: Dukes' type B
    Disease: colorectal adenocarcinoma
    Cellular Products: carcinoembryonic antigen (CEA) (The production of CEA in the ATCC seed stock was 1944 ng per 10(6) cells in 10 days.)
    interleukin 10 (IL-10) [22511 ]
    interleukin 6 (IL-6)
    mucin
    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
    Oncogene: myc +; myb + ; ras +; fos +; p53 +; sis -; abl -; ros -; src -
    Antigen Expression: serologically defined colon cancer antigen 3; Homo sapiens, expressed
    HLA A2, B13, B50; Blood type O
    DNA Profile (STR): Amelogenin: X
    CSF1PO: 10, 13, 14
    D13S317: 10
    D16S539: 11, 13
    D5S818: 11, 15
    D7S820: 11
    THO1: 6, 7
    TPOX: 8, 9
    vWA: 15, 17
    Cytogenetic Analysis: 45,X; one X chromosome missing; no other chromosomal aberrations
    Age: 58 years
    Gender: female
    Ethnicity: Caucasian
    Comments: LS 174T is a variant of LS 180 (ATCC CL-187 ) that has been maintained by using trypsin in the subculture protocol. It is more easily subcultivated than that parent line and, like LS 180, it is reported to produce large amounts of carcinoembryonic antigen (CEA).
    Electron microscopic studies revealed abundant microvilli and intracytoplasmic mucin vacuoles [Pubmed ID: 1262041].
    They are negative for p53 antigen expression, but positive for mRNA expression.
    LS 174T cells stain positively for cytokeratins.
    The line is positive for expression of c-myc, N-myc, H-ras, N-ras.
    Myb, and fos oncogenes.
    K-ras and sis oncogene expression were not detected.
    Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Eagle's Minimum Essential Medium, Catalog No. 30-2003. 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 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: 2 to 3 times per week
    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 30-2003
    recommended serum:ATCC 30-2020
    derived from same individual:ATCC CL-187
    References: 2148: Tom BH, et al. Human colonic adenocarcinoma cells. I. Establishment and description of a new line. In Vitro 12: 180-191, 1976. PubMed: 1262041
    3524: Tom BH, et al. Process of producing carcinoembryonic antigen. US Patent 4,228,236 dated Oct 14 1980
    22147: Chen TR, et al. Intercellular karyotypic similarity in near-diploid cell lines of human tumor origins. Cancer Genet. Cytogenet. 10: 351-362, 1983. PubMed: 6652615
    22511: Gastl GA, et al. Interleukin-10 production by human carcinoma cell lines and its relationship to interleukin-6 expression. Int. J. Cancer 55: 96-101, 1993. PubMed: 8344757
    22861: Trainer DL, et al. Biological characterization and oncogene expression in human colorectal carcinoma cell lines. Int. J. Cancer 41: 287-296, 1988. PubMed: 3338874
    32265: Tsao H, et al. Novel mutations in the p16/CDKN2A binding region of the Cyclin-dependent Kinase-4 gene. Cancer Res. 58: 109-113, 1998. PubMed: 9426066
    32377: Shibata D, et al. Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation. Nat. Genet. 6: 273-281, 1994. PubMed: 8012390
    32794: Kutchera W, et al. Protaglandin H synthase 2 is expressed abnormally in human colon cancer: evidence for a transcriptional effect. Proc. Natl. Acad. Sci. USA 93: 4816-4820, 1996. PubMed: 8643486

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    相关实验
    • 【求助】LS 174T 细胞培养问题

      chuenshui 细胞株:LS 174T 来源:中科院上海细胞库 培养基 :DMEM 10%小牛血清 问题:刚买回来时传代2次,都没问题。扩大培养时发现,细胞养起来时培养基发紫,0.25%胰酶消化传代,24小时候细胞50%不贴壁,细胞还呈发亮状态。 尝试解决办法:更换培养基,10小时后培养基发紫,细胞依然呈漂浮状态。无解决现象。 请问有什么办法可以解决,培养箱应该没问题,箱子里有同时培养的其他细胞,无异

    • CAR-T、MSC、T 细胞工艺流程图

      细胞治疗技术正扮演着越来越重要的角色。其中,CAR-T 细胞治疗、间充质干细胞(MSC)治疗以及 T 细胞治疗是三种备受关注的细胞治疗方法。 这些治疗方法通过采集患者体内的特定细胞,经过体外激活、修饰、扩增等步骤,再将这些具有特定功能的细胞移植回患者体内,以达到治疗疾病的目的。为了更好地理解和应用这些治疗技术,下面我们将整合并详细叙述这三种细胞治疗的流程图内容,为研究人员和临床医生提供一个清晰的操作指南。 CAR-T 细胞治疗流程 间充质干细胞治疗流程 T 细胞治疗流程  

    • t值表

      网络     附表3 t值表 n’ P(2): P(1): 0.50 0.25 0.20 0.10 0.10 0.05 0.05 0.025 0.02 0.01 0.01 0.005 0.005 0.0025 0.002 0.001 0.001

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