RHB-A: neural stem cell culture and differentiation medium
We are delighted to announce an exciting new partnership between TCS Biosciences and Takara Bio, bringing the renowned Cellartis® portfolio directly to researchers across the United Kingdom.
This collaboration strengthens our growing life science offering and provides UK scientists with easier access to Takara Bio's trusted stem cell technologies, supported by the dedicated service and technical expertise you expect from TCS Biosciences.
RHB-A is a fully defined, serum-free cell culture medium optimized for the derivation, maintenance, expansion, and differentiation of human and mouse neural stem (NS) cells. RHB-A is specifically formulated for culturing pure populations of adherent human and mouse NS cells. This medium ensures the long-term stability of NS cell differentiation capacity (Sun et al. 2008) and can be used to support differentiation of human and mouse NS cells into functional neurons (Sun et al. 2008; Conti et al. 2005; Hansen et al. 2010) and of mouse ES cells into neural precursors (Ying et al. 2003; Diogo, Henrique, and Cabral 2008; Abranches et al. 2009). Critically, RHB-A medium is more efficient at neural differentiation than conventional N2- and B27-based methods. RHB-A medium can be used to support organotypic slice culture of central nervous system tissues such as brain and spinal cord, and supports the culture of glioblastoma stem cells used in cancer research.
NOTE: RHB-A medium requires supplementation with Epidermal Growth Factor (EGF) and Fibroblast Growth Factor (FGF-2) for most applications (not supplied).
RHB-Basal medium does not contain any growth factors or neuronal supplements. Therefore, this medium can be tailored to the specific requirements of your cell type by the addition of supplements.
RHB-A, supplemented with Epidermal Growth Factor (EGF) and Fibroblast Growth Factor-2 (FGF-2), enables the maintenance and continual expansion of symmetrically-dividing NS cells in defined, serum-free adherent culture. In growth factor supplemented RHB-A, NS cells have been demonstrated to retain their neurogenic capacity for over 100 generations, with full maintenance of diploid karyotype. RHB-A in the presence of EGF and FGF-2 also supports the derivation of clonogenic NS cell lines. Culture of adherent NS cells in RHB-A with sequential growth factor withdrawal leads to differentiation into functional neurons. RHB-A supplemented with EGF and FGF-2 has recently been used for the propagation of glioblastoma stem cell lines.
Overview
- 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 free of animal components and neuronal supplements; the medium can be customized by the addition of supplements
Applications
- 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
- Organotypic slice culture of CNS tissue
- Glioblastoma stem cell culture for cancer research
- Refer to the Data Sheet for additional examples of use
References
Abranches, E. et al. Neural Differentiation of Embryonic Stem Cells In Vitro: A Road Map to Neurogenesis in the Embryo. PLoS One 4, e6286 (2009).
Conti, L. et al. Niche-Independent Symmetrical Self-Renewal of a Mammalian Tissue Stem Cell. PLoS Biol. 3, e283 (2005).
Diogo, M. M., Henrique, D. & Cabral, J. M. S. Optimization and integration of expansion and neural commitment of mouse embryonic stem cells. Biotechnol. Appl. Biochem. 49, 105 (2008).
Hansen, D. V., Lui, J. H., Parker, P. R. L. & Kriegstein, A. R. Neurogenic radial glia in the outer subventricular zone of human neocortex. Nature 464, 554–561 (2010).
Sun, Y. et al. Long-term tripotent differentiation capacity of human neural stem (NS) cells in adherent culture. Mol. Cell. Neurosci. 38, 245–258 (2008).
Ying, Q. L., Stavridis, M., Griffiths, D., Li, M. & Smith, A. Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture. Nat. Biotechnol. 21, 183–186 (2003).
Additional Information
Please refer to the product's Certificate of Analysis for detailed information on storage conditions, product components, and technical specifications. To view the contents of a kit, please consult the Kit Components List. Both documents can be found under the Documents tab on the Takara website, available here: https://www.takarabio.com/products/stem-cell-research
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