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      產(chǎn)品詳情
      • 產(chǎn)品名稱:CRL-2234 SNU-449 人肝癌細(xì)胞

      • 產(chǎn)品型號:CRL-2234 SNU-449
      • 產(chǎn)品廠商:美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      • 產(chǎn)品價格:0
      • 折扣價格:0
      • 產(chǎn)品文檔:
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      簡單介紹:
      CRL-2234 SNU-449 人肝癌細(xì)胞, ATCC 細(xì)胞|細(xì)胞系|細(xì)胞株|腫瘤細(xì)胞|細(xì)胞,細(xì)胞庫管理規(guī)范,提供 培養(yǎng)條件,
      詳情介紹:
      CRL-2234 SNU-449 人肝癌細(xì)胞

      SNU-449 (ATCC® CRL-2234)

      Permits and Restrictions

      View Restrictions

      Organism Homo sapiens, human
      Tissue
      liver
      Product Format frozen
      Morphology epithelial; diffusely spreading cells
      Culture Properties adherent              CRL-2234 SNU-449 人肝癌細(xì)胞
      Biosafety Level 2  [Cells contain Hepatitis B virus]
      Disease grade II-III/IV,hepatocellular carcinoma
      Age 52 years
      Gender male
      Ethnicity Asian
      Storage Conditions liquid nitrogen vapor phase
      Karyotype aneuploid; modal number = 57
      Derivation

      SNU-449 was derived in 1990 by J.-G. Park and associates from a primary hepatocellular carcinoma taken from a Korean patient prior to cytotoxic therapy.

      Tumor cells were initially cultured in ACL-4 medium supplemented with 5% heat inactivated fetal bovine serum. After establishment, cultures were maintained in RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum.
      Clinical Data
      52 years
      Asian
      male

      CRL-2234 SNU-449 人肝癌細(xì)胞
      Comments

      Hepatitis B virus (HBV) DNA was detected by Southern blot hybridization. HBV genomic RNA was not expressed.

      Grossly, the original tumor was single nodular with perinodular extensions. Histologically, it was predominantly compact and minor trabecular type.

      The cultured cells contain a single or double nucleus.
      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: heat-inactivated fetal bovine serum to a final concentration of 10%. 
       
      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 1:5 to 1:10 is recommended
      Medium Renewal: Every 2 to 3 days    CRL-2234 SNU-449 人肝癌細(xì)胞
      Cryopreservation
      Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
      Storage temperature: liquid nitrogen vapor phase
      Culture Conditions
      Atmosphere: air, 95%; carbon dioxide (CO2), 5%
      Temperature: 37°C

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