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        技術(shù)中心

        B16黑色素瘤細(xì)胞說明書

        2014年12月19日 10:37:23人氣:318來(lái)源:齊一生物科技(上海)有限公司

        資料類型jpg文件資料大小17222
        下載次數(shù)220資料圖片 【點(diǎn)擊查看】
        上 傳 人齊一生物科技(上海)有限公司 需要積分0
        關(guān) 鍵 詞B16黑色素瘤細(xì)胞說明書,B16黑色素瘤細(xì)胞
        【資料簡(jiǎn)介】

        B16(黑色素瘤細(xì)胞)  
         
        Cell Biology 
        ATCC® Number: CRL-6322™      Designations: B16-F0    
        Biosafety Level: 1 Shipped: frozen 
        Medium & Serum: See Propagation Growth Properties: adherent 
        Organism: Mus musculus (mouse) Morphology: Spindle shaped 
         
        Source: Organ: skin
        Disease: melanoma 
        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 ultimay responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location. 
        Related Cell Culture Products 
        Applications: transfection host (technology from amaxa
        Roche FuGENE® Transfection Reagents) 
        Tumorigenic: Yes, in syngeneic mice 
        Strain: C57BL/6J 
        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%.
        Temperature: 37.0C 
        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.
         
        Subc*tion ratio: A subc*tion ratio of 1:4 to 1:10 is recommended
         
        Medium renewal: Every 2 to 3 days
         
        Preservation: Freeze medium: Complete growth 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 30-2002
        recommended serum: ATCC 30-2020 
        References: 22151: Fidler IJ . Biological behavior of malignant melanoma cells correlated to their survival in vivo. Cancer Res. 35: 218-224, 1975. PubMed: 1109790
        22191: Fidler IJ , et al. Tumoricidal properties of mouse macrophages activated with mediators from rat lymphocytes stimulated with concanavalin A. Cancer Res. 36: 3608-3615, 1976. PubMed: 953987
        22192: Fidler IJ , Bucana C . Mechanism of tumor cell resistance to lysis by syngeneic lymphocytes. Cancer Res. 37: 3945-3956, 1977. PubMed: 908034
        22243: Fidler IJ , Kripke ML . Metastasis results from preexisting variant cells within a malignant tumor. Science 197: 893-895, 1977. PubMed: 887927
        22424: Fidler IJ . Immune stimulation-inhibition of experimental cancer metastasis. Cancer Res. 34: 491-498, 1974. PubMed: 4812256

         

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