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TAKARA Cellartis®干細(xì)胞研究產(chǎn)品-小鼠ES細(xì)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(xì)胞研究產(chǎn)品的全國代理商
TAKARA Cellartis®干細(xì)胞研究產(chǎn)品研發(fā)團(tuán)隊(duì)上百人，憑借20多年干細(xì)胞以及相關(guān)培養(yǎng)基研發(fā)經(jīng)驗(yàn)，研發(fā)并上市干細(xì)胞研究相關(guān)的多種產(chǎn)品，包括干細(xì)胞培養(yǎng)基，IPS干細(xì)胞系，干細(xì)胞分化細(xì)胞以及培養(yǎng)基，干細(xì)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).

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廠商性質(zhì)：代理商

更新時(shí)間：2025-02-13

訪問量：1114

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(xì)胞（NS）的定向分化獲取、維持培養(yǎng)、擴(kuò)增、誘導(dǎo)分化成神經(jīng)細(xì)胞等用途。RHB-A可用來培養(yǎng)擴(kuò)增貼壁的人或小鼠的神經(jīng)干細(xì)胞。在RHB-A中培養(yǎng)的神經(jīng)干細(xì)胞保持著穩(wěn)定的神經(jīng)干細(xì)胞分化發(fā)育成為成熟的神經(jīng)細(xì)胞的能力 (1-3) 。另外，RHB-A還用來定向分化小鼠胚胎干細(xì)胞(mouse ES)至神經(jīng)前體細(xì)胞 (neural precursors) (4-6)。
RHB‐Basal不包含生長因子或是神經(jīng)細(xì)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(rèn)為需要的添加物來開發(fā)適合客戶的特殊類型細(xì)胞的培養(yǎng)基。

■ 產(chǎn)品特點(diǎn)

· 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(xiàn)：

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,

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

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