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      產品詳情
      • 產品名稱:SW-13 人腎上腺皮質腺癌細胞

      • 產品型號:CCL-105
      • 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:
      CCL-105 SW-13 人腎上腺皮質腺癌細胞,原代細胞|細胞系|細胞株|菌種;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:
      CCL-105 SW-13 人腎上腺皮質腺癌細胞
      ATCC® Number: CCL-105?    Price: $323.00
      Designations: SW-13
      Depositors:  A Leibovitz
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Homo sapiens (human)
      Morphology: epithelial

      Source: Organ: adrenal gland
      Tissue: cortex
      Tumor Stage: grade IV
      Disease: primary small 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.
       
      Isolation: Isolation date: August, 1971
      Virus Susceptibility: Human poliovirus 1
      Vesicular stomatitis virus
      Reverse Transcript: negative
      DNA Profile (STR): Amelogenin: X
      CSF1PO: 11,12
      D13S317: 9
      D16S539: 12
      D5S818: 12
      D7S820: 8,10
      THO1: 7,8
      TPOX: 8
      vWA: 17,19
      Cytogenetic Analysis: modal number = 63; range = 45 to 65.
      Approximately 10% of the cells examined possessed a pair of dicentric chromosomes.
      Isoenzymes: G6PD, B
      Age: 55 years
      Gender: female
      Ethnicity: Caucasian
      Comments: Electron microscopic studies show many bulb gap junctions (BGJ).
      Propagation: ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Leibovitz's L-15 Medium, Catalog No. 30-2008. 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
      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 1:3 to 1:8 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 30-2008
      recommended serum:ATCC 30-2020
      References: 22140: . . In Vitro 8: 443, 1973.
      22526: Leibovitz A, et al. New human cancer cell culture lines. I. SW-13, small-cell carcinoma of the adrenal cortex. J. Natl. Cancer Inst. 51: 691-697, 1973. PubMed: 4765382
      22536: Fogh J, et al. Absence of HeLa cell contamination in 169 cell lines derived from human tumors. J. Natl. Cancer Inst. 58: 209-214, 1977. PubMed: 833871
      22539: Fogh J, et al. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J. Natl. Cancer Inst. 59: 221-226, 1977. PubMed: 327080
      23212: Lasfargues EY, Ozzello L. Cultivation of human breast carcinomas. J. Natl. Cancer Inst. 21: 1131-1147, 1958. PubMed: 13611537
      26278: Johnson RG, Sheridan JD. Junctions between cancer cells in culture: ultrastructure and permeability. Science 174: 717-719, 1971. PubMed: 4330805
      26279: Pinto da Silva P, Gilula NB. Gap junctions in normal and transformed fibroblasts in culture. Exp. Cell Res. 71: 393-401, 1972. PubMed: 4339896
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