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      產(chǎn)品詳情
      • 產(chǎn)品名稱:CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(xì)胞

      • 產(chǎn)品型號(hào):Detroit 562
      • 產(chǎn)品廠商:美國(guó)標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      • 產(chǎn)品價(jià)格:0
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      • 產(chǎn)品文檔:
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      簡(jiǎn)單介紹:
      CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(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,
      詳情介紹:
      CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(xì)胞
      Organism Homo sapiens, human
      Tissue pharynx: derived from metastatic site: pleural effusion
      Product Format frozen
      Morphology epithelial
      Culture Properties adherent
      Biosafety Level 1
      Disease pharyngeal carcinoma
      Age *****
      Gender female
      Ethnicity Caucasian
      Storage Conditions liquid nitrogen vapor phase
        Karyotype   Modal number = 64; range = 58 to128
      A large subterminal marker chromosome, arm ratio 3:4, is found in 94% of the cells karyotyped. Five to 6 minute chromosomes are present in each cell. Note: Cytogenetic information is based on initial seed stock at ATCC. Cytogenetic instability has been reported in the literature for some cell lines   Clinical Data  
      *****
      Caucasian
      female
        Genes Expressed  
      keratin
        Virus Susceptibility   Human poliovirus 1 
      Vesicular stomatitis virus               CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(xì)胞
        Comments  
      The cells are positive for keratin by immunoperoxidase staining.
      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%. 
       
      Subculturing

       

      Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes. 

      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.         CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(xì)胞
      Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
      Medium Renewal: Every 2 to 3 days
      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              CCL-138 Detroit 562 人咽頭癌胸水轉(zhuǎn)移細(xì)胞
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