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        1. 上海復(fù)祥生物科技有限公司

          當(dāng)前位置:上海復(fù)祥生物科技有限公司>>細(xì)胞庫(kù)>>人正常細(xì)胞>>CRL-11233™THLE-3 細(xì)胞,人肝永生化細(xì)胞

          THLE-3 細(xì)胞,人肝永生化細(xì)胞

          參   考   價(jià): ¥ 1

          訂  貨  量: ≥1 件

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          產(chǎn)品型號(hào):CRL-11233™

          品       牌:其他品牌

          廠商性質(zhì):生產(chǎn)商

          所  在  地:上海市

          更新時(shí)間:2024-11-15 12:43:41瀏覽次數(shù):1705

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          供貨周期 一周 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
          THLE-3 細(xì)胞,人肝永生化細(xì)胞
          ATCC 細(xì)胞|細(xì)胞系|細(xì)胞株|腫瘤細(xì)胞|細(xì)胞|貼壁細(xì)胞|懸浮細(xì)胞|,細(xì)胞庫(kù)管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻(xiàn)和培養(yǎng)條件

          THLE-3 細(xì)胞,人肝永生化細(xì)胞

          traces of serum which 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 with 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 0.1% Soybean Trypsin inhibitor  and aspirate cells by gently pipetting.

          5.To remove trypsin-EDTA solution, transfer cell suspension to centrifuge tube and spin at approximay 125 x g for 5 to 10 minutes.

          6.Discard supernatant and resuspend cells in fresh growth medium.  Add appropriate aliquots of cell suspension to new coated culture vessels.

          7.Place culture vessels in incubators at 37°C.

          Subc*tion Ratio: A subc*tion ratio of 1:3 to 1:6 is recommended

          Medium Renewal: Every 2 to 3 days

          THLE-3 細(xì)胞,人肝永生化細(xì)胞

          Flask Coating

          1.Prepare a mixture of 0.01 mg/mL fibronectin, 0.03 mg/mL bovine collagen type I and 0.01 mg/mL bovine serum albumin (BSA) dissolved in culture medium. Store pre-prepared Coating Solution at 4°C in cold room for up to 3 months.

          2.For a growth area of 75 cm2, add 4.5 mL of the fibronectin/collagen/BSA solution and rock gently to coat the entire surface.

          3.Incubate the freshly coated vessel(s) in a 37°C incubator overnight (it is preferable to use tissue culture vessels with tightened, plug-seal caps to prevent evaporation during the coating process).

          4.Store coated flasks with solution at room temperature, light protected, up to 1 month. Suction off solution before plating cells.


          Cryopreservation  Freeze medium: Complete growth medium, 95%; DMSO, 5%

          Storage temperature: liquid nitrogen vapor phase

          Culture Conditions  Temperature: 37°C

          STR Profile  Amelogenin: X

          CSF1PO: 11,12

          D13S317: 13

          D16S539: 11,12

          D5S818: 13

          D7S820: 8,10

          THO1: 8,9.3

          TPOX: 6,9

          vWA: 17,18

          Name of Depositor  National Cancer Institute

          References  Harris CC, et al. Human liver epithelial cells. US Patent 5,759,765 dated Jun 2 1998

          Pfeifer AM, et al. Simian virus 40 large tumor antigen-immortalized normal human liver epithelial cells express hepatocyte characteristics and metabolize chemical carcinogens. Proc. Natl. Acad. Sci. USA 90: 5123-5127, 1993. PubMed: 7685115

          Pfeifer AM, et al. Simian virus 40 large tumor antigen-immortalized normal human liver epithelial cells express hepatocyte characteristics and metabolize chemical carcinogens. Proc. Natl. Acad. Sci. USA 90: 5123-5127, 1993. PubMed: 7685115

          References  Harris CC, et al. Human liver epithelial cells. US Patent 5,759,765 dated Jun 2 1998

          Pfeifer AM, et al. Simian virus 40 large tumor antigen-immortalized normal human liver epithelial cells express hepatocyte characteristics and metabolize chemical carcinogens. Proc. Natl. Acad. Sci. USA 90: 5123-5127, 1993. PubMed: 7685115

          Pfeifer AM, et al. Simian virus 40 large tumor antigen-immortalized normal human liver epithelial cells express hepatocyte characteristics and metabolize chemical carcinogens. Proc. Natl. Acad. Sci. USA 90: 5123-5127, 1993. PubMed: 7685115





















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