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      產(chǎn)品詳情
      • 產(chǎn)品名稱:NCI-N87 [N87] 人胃癌細胞

      • 產(chǎn)品型號:CRL-5822
      • 產(chǎn)品廠商:美國標(biāo)準(zhǔn)生物品收藏中心(ATCC)
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      CRL-5822 NCI-N87 [N87] 人胃癌細胞,原代細胞|細胞系|細胞株|菌種;細胞庫管理規(guī)范,提供的細胞株背景清楚,提供參考文獻和培養(yǎng)條件!
      詳情介紹:

      CRL-5822 NCI-N87 [N87] 人胃癌細胞
      ATCC® Number:  CRL-5822?      
      Designations:  NCI-N87 [N87] 
      Depositors:   J Park 
      Biosafety Level: 1 
      Shipped:  frozen 
      Medium & Serum:  See Propagation 
      Growth Properties: adherent
      Organism: Homo sapiens (human) 
      Morphology: epithelial

       
      Source: Organ: stomach
      Disease: gastric carcinoma
      Derived from metastatic site: liver
      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: 1976
      Receptors: acetylcholine, muscarinic, expressed [23078]
      Tumorigenic: Yes 
      Oncogene: myc +; erb B2 + 
      DNA Profile (STR): Amelogenin: X,Y
      CSF1PO: 8,12
      D13S317: 8,11
      D16S539: 9,13
      D5S818: 12,13
      D7S820: 10,11
      THO1: 9
      TPOX: 9,11
      vWA: 15,16
      Cytogenetic Analysis: near diploid; DM were present in 64% of cells examined
      Gender:  male 
      Comments: NCI-N87 cells express the surface glycoproteins carcinoembryonic antigen (CEA) and TAG 72, and are L-dopa decarboxylase (DDC) negative. They were minimally positive for vasoactive intestinal peptide (VIP) receptors and lacked gastrin receptors. They were fiound to express receptors for muscarinic cholinergic agents. No evidence of amplification or rearrangements was noted with the N-myc, L-myc, myb and EGF receptor genes. The cell line expressed levels of c-myc and c-erb-B 2 RNA that were comparable to other cell lines.There was no expression of the following genes: N-myc, L-myc, c-cis, IGF-2, or gastrin releasing peptide. NCI-N87 cells have a reported plating efficiency of 4.3%.
      Propagation:  ATCC complete growth medium: The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. 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
      Growth Conditions: They grow as an adherent monolayer of tightly knit epithelial cells.
      Subculturing:  Protocol:
      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 that 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 1:3 to 1:4 is recommended
      Medium Renewal: Two to three times weekly
      Preservation:  Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
      Storage temperature: liquid nitrogen vapor phase
      Doubling Time:  47 hrs 
      Related Products: Recommended medium (without the additional supplements or serum described under ATCC Medium):ATCC 30-2001
      recommended serum:ATCC 30-2020
      References: 23078: Park JG, et al. Characteristics of cell lines established from human gastric carcinoma. Cancer Res. 50: 2773-2780, 1990. PubMed: 2158397
      23570: . NCI-Navy Medical Oncology Branch Cell Line Supplement. J. Cell. Biochem. suppl. 24: 1996..
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