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      產(chǎn)品詳情
      • 產(chǎn)品名稱:HIT-T15 大鼠胰腺B細(xì)胞

      • 產(chǎn)品型號:CRL-1777
      • 產(chǎn)品廠商:美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
      • 產(chǎn)品價格:0
      • 折扣價格:0
      • 產(chǎn)品文檔:
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      簡單介紹:
      HIT-T15 大鼠胰腺B細(xì)胞,原代細(xì)胞|細(xì)胞系|細(xì)胞株|菌種;細(xì)胞庫管理規(guī)范,提供的細(xì)胞株背景清楚,提供參考文獻和Z優(yōu)培養(yǎng)條件!
      詳情介紹:
      HIT-T15   大鼠胰腺B細(xì)胞
      ATCC® Number: CRL-1777?    Price: $289.00
      Designations: HIT-T15
      Depositors:  R Santerre
      Biosafety Level: 2 [Cells Contain PAPOVAVIRUS ]
      Shipped: frozen
      Medium & Serum: See Propagation
      Growth Properties: adherent
      Organism: Mesocricetus auratus (hamster, Syrian golden)
      Morphology: epithelial
      HIT-T15 大鼠胰腺B細(xì)胞
      Source: Organ: pancreas
      Tissue: islet of Langerhans
      Cell Type: beta cell;
      Cellular Products: insulin
      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: glucagon; somatostatin; glucocorticoid
      Comments: This line was established from a primary culture of Syrian hamster islet cells which were transformed with SV40.
      The cells secrete up to 24 ng of insulin per 10 exp6 cells per 24 hours (passage 60).
      Insulin secretion is stimulated by glucose and glucagon, and is suppressed by somatostatin and glucocorticoids.
      Insulin synthesis decreases with length of time in culture.
      Propagation: ATCC complete growth medium: Ham's F12K medium with 2 mM L-glutamine adjusted to contain 1.5 g/L sodium bicarbonate, 87.5%; dialyzed horse serum, 10%; 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 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.
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