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    當(dāng)前位置:主頁 > 產(chǎn)品中心 > > >TAKARA Cellartis®干細胞研究產(chǎn)品-小鼠ES細胞神經(jīng)分化培養(yǎng)基 RHB-A&

    TAKARA Cellartis®干細胞研究產(chǎn)品-小鼠ES細胞神經(jīng)分化培養(yǎng)基 RHB-A&

    簡要描述:熱烈祝賀華雅生物成為TAKARA Cellartis®干細胞研究產(chǎn)品的全國代理商
    TAKARA Cellartis®干細胞研究產(chǎn)品研發(fā)團隊上百人,憑借20多年干細胞以及相關(guān)培養(yǎng)基研發(fā)經(jīng)驗,研發(fā)并上市干細胞研究相關(guān)的多種產(chǎn)品,包括干細胞培養(yǎng)基,IPS干細胞系,干細胞分化細胞以及培養(yǎng)基,干細胞檢測抗體等;產(chǎn)品品種豐富,*,具有配方和*的產(chǎn)品特質(zhì).

    • 產(chǎn)品型號:
    • 廠商性質(zhì):代理商
    • 更新時間:2025-02-13
    • 訪  問  量:1200
    詳細介紹
    Neural Stem Cell Culture Media
    RHB-A和RHB-Basal是兩款無血清、成分*確定的培養(yǎng)基,用于人類或小鼠神經(jīng)干細胞(NS)的定向分化獲取、維持培養(yǎng)、擴增、誘導(dǎo)分化成神經(jīng)細胞等用途。RHB-A可用來培養(yǎng)擴增貼壁的人或小鼠的神經(jīng)干細胞。在RHB-A中培養(yǎng)的神經(jīng)干細胞保持著穩(wěn)定的神經(jīng)干細胞分化發(fā)育成為成熟的神經(jīng)細胞的能力 (1-3) 。另外,RHB-A還用來定向分化小鼠胚胎干細胞(mouse ES)至神經(jīng)前體細胞 (neural precursors) (4-6)。
    RHB‐Basal不包含生長因子或是神經(jīng)細胞相關(guān)的添加物。因此,可以RHB‐Basal為基礎(chǔ),通過添加客戶認為需要的添加物來開發(fā)適合客戶的特殊類型細胞的培養(yǎng)基。
     
    ■ 產(chǎn)品特點
    · RHB-A is a proprietary, fully defined, and serum-free medium designed to maintain pure populations of adherent 
       human and mouse NS cells
    · RHB-Basal medium is animal component-free and contains no neuronal supplements; the media can be 
       customized by the addition of supplements 
     
    ■ 產(chǎn)品應(yīng)用
    · Derivation of mouse and human NS cells from ES cells and fetal and adult tissues
    · Maintenance and propagation of adherent mouse and human NS cells
    · Differentiation of mouse and human NS cells into functional neurons 
    · Differentiation of mouse ES cells to neuronal precursors 
    · Refer to the Data Sheet for additional examples of use
     

    ■ 產(chǎn)品詳情

     
    Adherent mouse neural stem cells cultured in RHB-A medium supplemented with epidermal growth factor and fibroblast growth factor-2 express neural stem cell markers, including Nestin, Vimentin (3CB2), radial glial cell marker-2 (RC2), glial fibrillary acidic protein (GFAP), and microtubule associate protein (MAP).
     
    參考文獻:
    1. Ying QL, et al. (2003) Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture. 
        Nature Biotechnology 21:183-186.
    2. Conti L, et al. (2005) Niche-Independent symmetrical self-renewal of a mammalian tissue stem cell. 
        PLoS Biology 3(9):e283.
    3. Pollard SM, et al. (2006) Adherent Neural Stem (NS) cells from fetal and adult forebrain. Cerebral Cortex 16:112-120.
    4. Diogo MM, et al. (2008) Optimization and integration of expansion and neural commitment of mouse embryonic stem cells.
        Biotechnology and Applied Biochemistry 49:105-112.
    5. Pollard SM, et al. (2008) Fibroblast growth factor induces a neural stem cell phenotype in foetal forebrain progenitors 
        and during embryonic stem cell differentiation. Molecular and Cellular Neuroscience 38:393:403.
    6. Sun Y, et al. (2008) Long-term tripotent differentiation capacity of human neural stem (NS)cells in adherent culture. 
        Molecular and Cellular Neuroscience 38:245-258.
    7. Pollard SM, et al. (2009) Glioma stem cell lines expanded in adherent culture have tumor-specific phenotypes and are 
        suitable for chemical and genetic screens. Cell Stem Cell 4:568-580.
    8. Abranches E, et al. (2009) Neural differentiation of embryonic stem cells in vitro: A road map to neurogenesis 
        in the embryo. PLoS ONE 4(7): e6286.
    9. Fernandes et al. (2010) Hypoxia enhances proliferation of mouse embryonic stem cell-derived neural stem cells.
        Biotechnology and Bioengineering 106: 260–270.
    10. Fernandes, T.G., et al. (2010) Different stages of pluripotency determine distinct patterns of proliferation, metabolism, 

     


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