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      正常小鼠睪丸Sertoli細胞

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      產品名稱: 正常小鼠睪丸Sertoli細胞
      產品型號: CRL-1715
      產品廠商: 美國標準生物品收藏中心(ATCC)
      產品文檔: 無相關文檔


      簡單介紹

      CRL-1715 TM4 正常小鼠睪丸Sertoli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*優培養條件!


      正常小鼠睪丸Sertoli細胞 的詳細介紹
      CRL-1715 TM4 正常小鼠睪丸Sertoli細胞
      ATCC® Number: CRL-1715?    Price: $329.00
      Designations: TM4
      Depositors:  JP Mather
      Biosafety Level: 1
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Mus musculus (mouse)
      Morphology: epithelial

      Source: Organ: testis
      Disease: normal
      Cell Type: Sertoli cell;
      Cellular Products: retinol binding protein
      tissue plasminogen activator
      transferrin
      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.
       
      Applications: transfection host (Roche FuGENE® Transfection Reagents)
      Receptors: follicle stimulating hormone (FSH), expressed
      androgen receptor, expressed
      progesterone receptor, expressed
      Tumorigenic: No
      Antigen Expression: H-Y antigen; Mus musculus, expressed
      Age: 11 to 13 days
      Gender: male
      Comments: The TM4 cell line is reported to respond to FSH with an increase in cAMP production, but to not respond to luteinizing hormone (LH). The FSH responsiveness is much reduced compared to primary sertoli cell cultures. Constitutive plasminogen activator production is reported to be low, but is stimulated by FSH and, to a greater extent, by retinoic acid.
      Tested and found negative for ectromelia virus (mousepox).
      Propagation: ATCC complete growth medium: A 1:1 mixture of Ham'S F12 medium and Dulbecco's modified Eagle's medium with 1.2 g/L sodium bicarbonate and 15 mM HEPES, 92.5%; horse serum, 5%; fetal bovine serum, 2.5%
      Atmosphere: air, 95%; carbon dioxide (CO2), 5%
      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 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 37C 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 supension to new culture vessels.
      6. Incubate cultures at 37C.

      Subcultivation Ratio: A subcultivation ratio of 1:10 to 1:50 is recommended
      Medium Renewal: Every 3 to 4 days
      Preservation: Freeze medium: Culture 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 30-2006
      recommended serum:ATCC 30-2020
      recommended serum:ATCC 30-2040
      References: 1158: Mather JP. Establishment and characterization of two distinct mouse testicular epithelial cell lines. Biol. Reprod. 23: 243-252, 1980. PubMed: 6774781
      1159: Mather JP, et al. Culture of testicular cells in hormone-supplemented serum-free medium. Ann. N.Y. Acad. Sci. 383: 44-68, 1982. PubMed: 7046561
      1184: Carson DD, et al. Synthesis and secretion of a novel binding protein for retinol by a cell line derived from Sertoli cells. J. Biol. Chem. 259: 3117-3123, 1984. PubMed: 6538197
      26150: Mather JP, Phillips DM. Establishment of a peritubular myoid-like cell line and interactions between established testicular cell lines in culture. J. Ultrastruct. Res. 87: 263-274, 1984. PubMed: 6544874
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