Quick-Neuron™ Dopaminergic – Human iPSC-Derived Neurons (Healthy Donor)

Quick-Neuron™ Dopaminergic are cryopreserved, ready-to-use human iPSC-derived dopaminergic neurons that provide a consistent, biologically relevant in vitro model of human dopaminergic neuronal function. These off-the-shelf human iPSC-derived dopaminergic neurons are generated using a proprietary mRNA-based reprogramming method, ensuring rapid maturation and a genetic footprint-free workflow. Ideal for Parkinson’s disease modeling, dopamine signaling studies, neurodegenerative disease research, drug discovery, and neurotoxicity screening, Quick-Neuron™ Dopaminergic delivers reproducible performance across neuronal network activity assays and downstream characterization workflows.

SKU: DA-mRNA-HC-CW50065 Categories: , ,

$1,100.00

Advantages of iPSC-Derived Dopaminergic Neurons

Rapid Differentiation
~7 days
Functionally Validated
QC confirmed
Highly Pure Population
TH+, TUBB3+
No Genetic Footprint
0 modifications

Dopaminergic Neuron Protocol

Our step-by-step protocol guides the efficient and reproducible differentiation of dopaminergic neurons from human induced pluripotent stem cells (iPSCs). Designed for ease of use, this protocol supports robust neuronal induction and maturation, helping researchers generate physiologically relevant dopaminergic populations for disease modeling and drug discovery.

DA mRNA CW workflow
Phase contrast imagery of dopaminergic neurons on day 1 at 4x magnification
dopaminergic neurons phase contrast day 1 10x

Day 1

Phase contrast imagery of dopaminergic neurons on day 2 at 4x magnification
dopaminergic neurons phase contrast day 2 10x

Day 2

dopaminergic neurons phase contrast day 3 4x
dopaminergic neurons phase contrast day 3 10x

Day 3

dopaminergic neurons phase contrast day 6 4x
dopaminergic neurons phase contrast day 6 10x

Day 6

Dopaminergic neuron morphology is confirmed via phase contrast imagery: Representative phase contrast images of Quick-Neuron™ Dopaminergic – human iPSC-derived neurons on days 1-6 post-thaw.

Dopaminergic Neuron Characterization

Quick-Neuron™ Dopaminergic – Human iPSC-Derived Dopaminergic Neurons undergo rigorous characterization via immunofluorescent staining for key dopaminergic neuron markers. This process confirms cell identity, purity, and functionality to ensure reliable performance in downstream applications such as disease modeling and neurotoxicity screening.

Dopaminergic Neuron Marker Expression

Characterization of Quick-Neuron™ Dopaminergic includes immunofluorescent staining for tyrosine hydroxylase (TH), the pan-neuronal marker TUBB3, and nuclear staining with Hoechst 33342. This combination confirms dopaminergic identity, neuronal lineage, and cell count, supporting confident use in applications such as disease modeling, drug screening, and neurotoxicity assessment.

dopaminergic neurons immunocytochemistry icc

iPSC-derived dopaminergic neurons express neuronal markers and display typical neurite growth. Immunofluorescent staining of Quick-Neuron™ Dopaminergic – mRNA Kit cell cultures shows typical neurite growth and expression of the pan-neuronal marker TUBB3 and the dopaminergic neuron-specific marker TH on day 7 post-differentiation. Nuclei were counterstained with Hoechst 33342. (scale bars = 100 μm).

Product Specifications

Parameters Specifications
Product Name Quick-Neuron™ Dopaminergic - Human iPSC-Derived Neurons
Catalog No. DA-mRNA-HC-CW50065
Product Components Cryopreserved cells, Component N, Component P, Component D4, Component D5, and Component D6
Starting Material iPSCs derived from peripheral blood mononuclear cells (CIRM line CW50065)
Storage Conditions Frozen cells should be stored in liquid nitrogen (vapor phase). The rest of the components should be stored at -20°C.
Cell Type Dopaminergic Neurons
Culture Type Feeder Cell-Free
Disease Healthy Donor
Donor Sex Female
Donor Age at Sampling 74
Donor Race Ethnicity Caucasian, not Latino
Patient History See Resources for more information.
Reprogramming Method Episomal vector
Induction Method Transcription factors delivered by synthetic mRNA
Growth Properties Adherent
Number of viable cells > 1.0 million viable cells per vial upon thawing
Cell viability and remaining live cells >50% at day 1, >211 live cells per mm2
>50% at day 7, >211 live cells per mm2
Differentiation At day 7 post-differentiation (CW50065)
>80% TUBB3+,
>50% TH+/TUBB3+
Sterility No growth observed
Mycoplasma No mycoplasmal enzymes detected
Morphological Observation Cells are adherent and neurites exhibit substantial outgrowth, elongation and branching, indicative of a differentiated phenotype.
Restricted Use For research use only. Not for use in diagnostic or therapeutic procedures.

Dopaminergic Neuron Resources

Induction of specific neuron types by overexpression of single transcription factors.

Synthetic mRNA-based differentiation method enables early detection of Parkinson’s phenotypes in neurons derived from Gaucher disease-induced pluripotent stem cells.

Versatile live-cell activity analysis platform for characterization of neuronal dynamics at single-cell and network level.

Efficient derivation and banking of clinical-grade human embryonic stem cell lines in accordance with Japanese regulations

No results found.

FAQs

Does Quick-Tissue™ technology leave a genetic footprint?

Sendai virus (SeV) is an RNA virus, so it does not integrate into the genomic DNA. In principle, a foreign gene introduced intracellularly in the form of RNA is quickly translated and expressed because, unlike DNA, RNA does not need to enter the nucleus for forced expression, thereby providing no chance of mutagenesis. This is discussed in the following review paper: Yamamoto, et al., (2009) “Current prospects for mRNA gene delivery.” Eur. J. Pharm Biopharm 71, 484-489.

Will SeV remain active after differentiation?

No. The SeV used in our kits is a temperature-sensitive mutant that is active at 33℃ but becomes inactive at 37℃, which is the temperature instructed in the user guides post-differentiation.

Is Sendai virus (SeV) dangerous?

SeV is not pathogenic to humans (i.e., humans are not the natural host of the virus) and the infection does not persist in immunocompetent animals. Furthermore, SeV used in our kits does not produce infectious viral particles upon transduction to host hPSCs and is a temperature-sensitive mutant, such that it is active at 33℃ but becomes inactive at 37℃. However, because SeV can be transmitted by aerosol and contact with respiratory secretions and is highly contagious, appropriate care must be taken to prevent potential mucosal exposure to the virus. Our SeV-based kits must be used under Biosafety Level 2 (BL-2) containment with a biological safety cabinet or a laminar flow hood and with appropriate personal protective equipment. In the event that the virus comes into contact with skin or eyes, decontaminate the affected area by flushing with plenty of water and follow the safety manual prepared by your laboratory and approved by your Institutional Biosafety Committee.

Do I need a license agreement for any of Ricoh Biosciences’ products?

No. You don’t need any licence or material transfer agreement (MTA) to use our differentiation kits or iPSC-derived cells. However, please be advised that these products are for research use only.

No results found.

Contact Us

Have a question about our products, services, or custom projects? Our team is here to help—reach out and we’ll get back to you as soon as possible.

Subscribe

Sign up to our eNewsletter to stay up to date with the latest product launches, promotions, and receive expert tips.

By signing up you are agreeing to our Privacy Policy