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Efficient generation of dopamine neurons from human embryonic stem cells.

Methods in molecular biology (Clifton, N.J.) (2008-05-06)
Chang-Hwan Park, Sang-Hun Lee
要旨

In this chapter, we introduce a co-culture protocol for human embryonic stem (hES) cell differentiation in which dopamine (DA) neurons with midbrain-specific markers are efficiently derived. Human ES cells on a feeder layer of stromal cells are induced to differentiate into neuroepithelial or neural precursor cells with embryonic midbrain precursor properties. The resulting neural precursor cells are then selectively expanded and serially passaged to obtain a large, homogeneous population of these cells. Under the conditions for terminal differentiation, the majority of hES-derived neural precursors differentiate into neuronal cells that are positive for DA neuronal markers such as tyrosine hydroxylase (TH) and function in vitro as presynaptic DA neurons.

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Sigma-Aldrich
ウシ血漿フィブロネクチン, solution, sterile-filtered, BioReagent, suitable for cell culture
Sigma-Aldrich
重炭酸ナトリウム, powder, BioReagent, for molecular biology, suitable for cell culture, suitable for insect cell culture
Sigma-Aldrich
ゼラチン from porcine skin, powder, gel strength ~300 g Bloom, Type A, BioReagent, suitable for electrophoresis, suitable for cell culture
Sigma-Aldrich
亜セレン酸ナトリウム, BioReagent, suitable for cell culture, ≥98%
Sigma-Aldrich
アポトランスフェリン ヒト, powder, BioReagent, suitable for cell culture, ≥98% (agarose gel electrophoresis)