Quick-Neuron™ Dopaminergic – Maintenance Medium
Quick-Neuron™ Dopaminergic – Maintenance Medium is formulated for long-term maintenance of human iPSC-derived dopaminergic neurons in vitro. Designed for research use, this medium supports consistent culture performance for downstream neuroscience and neuropharmacology applications.
$220.00
Product Specifications
| Parameters | Specifications |
|---|---|
| Product Name | Quick-Neuron™ Dopaminergic - Maintenance Medium |
| Catalog No. | DA-MM |
| Product Components | Component N, Component D4, Component D6, and Component P |
| Storage Conditions | All components can be stored at -20°C or -80°C. |
| Cell Type | Dopaminergic Neurons |
| Shelf Life | 1 Year |
| Sterility | No growth observed for Bacteria and Fungus |
| Mycoplasma | No contamination detected |
| Restricted Use | For research use only. Not for use in diagnostic or therapeutic procedures. |
Dopaminergic Neuron Resources
Quick-Neuron™ Dopaminergic – Human iPSC-Derived Neurons
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.
Related Products
FAQs
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.
What kind of transcription factors are used for differentiation induction?
It is a proprietary formulated RNA and cannot be disclosed.
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.
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