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      產品詳情
      • 產品名稱:CRL-1749 UM-UC-3 人膀胱移行細胞癌

      • 產品型號:CRL-1749 UM-UC-3
      • 產品廠商:美國標準生物品收藏中心(ATCC)
      • 產品價格:0
      • 折扣價格:0
      • 產品文檔:
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      簡單介紹:
      CRL-1749 UM-UC-3 人膀胱移行細胞癌,ATCC 細胞|細胞系|細胞株|腫瘤細胞|細胞;細胞庫管理規范,提供的細胞株背景清楚,提供參考文獻和培養條件!
      詳情介紹:
      CRL-1749 UM-UC-3 人膀胱移行細胞癌
      ATCC® Number: CRL-1749™ Price:
      See New Benefits of ATCC Culture
      Designations: UM-UC-3
      Depositors: HB Grossman
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Homo sapiens
      Morphology: epithelial

      Source: Organ: urinary bladder
      Disease: transitional cell carcinoma
      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
      DNA Profile (STR): Amelogenin: X
      CSF1PO: 10,11
      D13S317: 8
      D16S539: 8,9
      D5S818: 12
      D7S820: 8,9
      THO1: 6,9
      TPOX: 10
      vWA: 17
      Cytogenetic Analysis: This is a hypertriploid human cell line. The modal chromosome number was 80, occurring in 42% of cells. Cells with 78 chromosomes also occurred at a high frequency. The rate of cells with higher ploidies was 2.5%. There were 30 or more marker chromosomes in each cell. They included der(1)t(1;?) (p32;?), ?t(1p5p), i(3q), t(7q14q), ?t(2p3p) and others. The X and N3 had single copy per cell, and others were generally two to three copies per cell.
      Gender: male
      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%.
      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 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 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 1:4 to 1:10 is recommended
      Medium Renewal: 2 to 3 times per week
      Preservation: Freeze medium: Complete growth medium, 95%; DMSO, 5%
      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
      References: 25065: Bellet D, et al. Malignant transformation of nontrophoblastic cells is associated with the expression of chorionic gonadotropin beta genes normally transcribed in trophoblastic cells. Cancer Res. 57: 516-523, 1997. PubMed: 9012484
      26153: Grossman HB, et al. Improved growth of human urothelial carcinoma cell cultures. J. Urol. 136: 953-959, 1986. PubMed: 3761468
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