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      H9c2(2-1) 大鼠心肌細胞

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      產品名稱: H9c2(2-1) 大鼠心肌細胞
      產品型號: CRL-1446
      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-1446 H9c2(2-1) 大鼠心肌細胞,原代細胞|細胞系|細胞株|菌種原代細胞、細胞系。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


      H9c2(2-1) 大鼠心肌細胞 的詳細介紹

      CRL-1446 H9c2(2-1) 大鼠心肌細胞
      ATCC® Number:  CRL-1446?      
      Designations:  H9c2(2-1) 
      Depositors:   W Carlisle 
      Biosafety Level: 1 
      Shipped:  frozen 
      Medium & Serum:  See Propagation 
      Growth Properties: adherent
      Organism: Rattus norvegicus (rat) 
      Morphology: myoblast

       
      Source: Strain: BD1X
      Organ: heart
      Tissue: myocardium
      Cellular Products: myokinase; creatine phosphokinase; myosin 
      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: acetylcholine, expressed
      Age:  embryo 
      Comments: H9c2(2-1) is a subclone of the original clonal cell line derived from embryonic BD1X rat heart tissue by B. Kimes and B. Brandt and exhibits many of the properties of skeletal muscle.
      Myoblastic cells in this line will fuse to form multinucleated myotubes and respond to acetylcholine stimulation.
      Fusion occurs faster if the serum concentration in the medium is reduced to one percent.
      Propagation:  ATCC complete growth medium: The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
      Atmosphere: air, 95%; carbon dioxide (CO2), 5%
      Temperature: 37.0°C
      Subculturing:  Protocol: The myoblastic population will become depleted rapidly if the cultures are allowed to become confluent.
      To prevent loss of myoblastic cells, cultures should be subcultured before they become confluent, and the line should be recloned periodically with selection for myoblastic cells.

      Remove and discard culture medium.
      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.
      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.
      Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting.
      Add appropriate aliquots of the cell suspension to new culture vessels.
      Incubate cultures at 37°C.

      Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended
      Medium Renewal: Every 2 to 3 days
      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 30-2002
      recommended serum:ATCC 30-2020
      References: 1062: Kimes BW, Brandt BL. Properties of a clonal muscle cell line from rat heart. Exp. Cell Res. 98: 367-381, 1976. PubMed: 943302
      32970: Levy AP, et al. Post-transcriptional regulation of vascular endothelial growth factor by hypoxia. J. Biol. Chem. 271: 2746-2753, 1996. PubMed: 8576250 
       
       

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