Human Dopaminergic Neurons (iPSC-derived, Normal)

Description Product Code Price Quantity Add to Cart
Cryopreserved, 1.0 million cells/vial
Cryopreserved, 2.0 million cells/vial

Product Overview

Midbrain dopamine (DA) neurons are critical for directing fundamental brain functions such voluntary movement, reward processing, and working memory. The substantia nigra (SN) and the ventral tegmental area (VTA) have the highest populations of DA neurons in the midbrain. The degeneration of DA neurons within the pars compacta region of the SN is a pathological hallmark of Parkinson’s disease (PD) and Lewy body dementia (LBD) [1]. For many years, powerful experimental model organisms like the mouse, fruit fly, and baker's yeast have been used to study neurodegenerative diseases, providing insights into disease mechanisms like pathological aggregation of key proteins, the nature and processes of neuronal damage, the role of genetic determinants, and the contribution of neuroinflammation in fueling neuronal loss [2,3]. However, it appears that the use of these models has only partially elucidated some elements of the illnesses, impeding a meaningful translation into new treatments, diagnostics, and prevention.

iXCells Biotechnologies is proud to provide fully differentiated and functional human iPSC-derived DA neurons that display typical neuronal morphology and express all key markers of DA neurons, e.g., TH, FoxA2 (Figure 1) when cultured in the Human Dopaminergic Neuron Maturation Medium (Cat# MD-0105-100ML). In addition, our iPSC-derived DA neurons can also be co-cultured with glial cells or other cell types for drug screening platforms.

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Figure 1. Human iPSCs derived dopaminergic neurons show expression of characteristic biological markers. (A) Immunostaining shows the expression of midbrain dopaminergic neuron markers FoxA2 and TH, 28 days post-thawing. (B) Quantifications for percentage of dopaminergic neurons, positive for the TH marker over multiple time-points. Results are expressed as means ± SEM. (C) Flow cytometry measurements demonstrate a highly specific population of fully differentiated midbrain dopaminergic neuron (TH). (D)(E) Immunostaining shows the expression of neuron marker TuJ1 (D) 21 days post-thawing and MAP2 (E) 7 days post-thawing and the absence of the proliferative progenitor marker Ki67. (F) Flow cytometry measurements demonstrate a highly pure population of fully differentiated neurons (MAP2). Nuclei were counterstained with DAPI. Scale bars, 200 µm.

Product Details


  Human iPSC-derived dopaminergic neurons (Normal)

  Package Size

  1.0 million cells/vial; 2.0 million cells/vial;




  Liquid Nitrogen


 Human Dopaminergic Neuron Maturation Medium (Cat # MD-0105-100ML)


Product Information



[1] Bloem, B. R., Okun, M. S. & Klein, C. (2021) Parkinson’s disease. Lancet 397, 2284–2303.

[2] Schulz-Schaeffer, W.J. (2015). Is Cell Death Primary or Secondary in the Pathophysiology of Idiopathic PD? Biomolecules 5, 1467-1479.

[3] Poewe, W., Seppi, K., Tanner, C. et al. (2017). Parkinson disease. Nat Rev Dis Primers 3, 17013

Species Homo Sapiens



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