Quick-Neuron™ Excitatory – SeV Kit

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Quick-Neuron™ Excitatory – SeV Kit

This kit differentiates human pluripotent stem cells into excitatory neurons in 10 days using Sendai virus.

Note: This kit is no longer available for individual sale. We now offer bulk orders and custom differentiation services.

Advantages of iPSC-Derived Excitatory Neurons

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~ 1 Week Differentiation

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Optimized & Reproducible

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Highly Pure Population

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No Genetic Footprint

Excitatory Neuron Differentiation Kit Protocol

Explore our detailed differentiation protocols, a step-by-step guide designed to simplify and optimize your laboratory procedures using our iPSC-derived cells and differentiation kits. These protocols leverage the latest advancements in iPSC technology to ensure efficient and reproducible results.

excitatory neuron SeV kit workflow
excitatory neuron SeV kit phase contrast

Excitatory Neuron morphology is confirmed via phase contrast imagery: Representative images of Quick-Neuron™ Excitatory – SeV Kit cell cultures on days 1-10 post-differentiation (scale bar = 100 μm).

Excitatory Neuron Characterization

Characterization of iPSC-derived excitatory neurons is crucial to ensure their utility in research. Employing excitatory neuron markers, researchers can confirm the identity and purity of these neurons.

Excitatory Neuron Marker Expression

Understanding the role of excitatory neuron markers is crucial in neuroscience research. Our comprehensive guide delves into the identification and significance of these markers in iPSC-derived neurons, providing essential information for researchers.
Excitatory Neuron Marker Expression

iPSC-derived excitatory neurons express neuronal markers and display typical neurite growth. Immunofluorescent staining of Quick-Neuron™ Excitatory – Human iPSC-derived Neurons on Day 7 post-thaw that shows expression of the pan-neuronal marker TUBB3 and the glutamatergic neuron marker vGLUT1 (scale bar = 100 μm).

Excitatory Neuron Electrophysiology

Whole-Cell Patch Clamp 

Whole Cell Patch Clamp

Electrophysiological properties of iPSC-derived excitatory neurons. Whole-cell patch clamp of Quick-Neuron™ Excitatory – Human iPSC-derived Neurons 5-6 weeks post-thaw. (A) A brightfield image of the neurons measured. (B) Spontaneous action potentials were recorded. (C) Spontaneous excitatory postsynaptic current of neurons was detected by voltage clamp measurement at -70mV, indicating the formation of mature synapses. Data courtesy of E-PHY SCIENCE SAS.

Multi-Electrode Array (MEA)

Multi Electrode Array (MEA)

Excitatory Neurons seeded onto MEA plates remain functional after transport. An MEA plate seeded with Quick-Neuron™ Excitatory Neurons and primary human astrocytes was transported from Tokyo, Japan to Maryland, USA. The baseline network burst firing of one well was measured on day 49 post-thaw before transport (A) and on day 50 after 33-hr transport (B). (C) Network burst firing on day 51 exhibited responses to varying concentrations of 4-AP after transport. Data courtesy of Ricoh.

RNA-Sequencing

RNA Sequencing

Gene Expression of Quick-Neuron™ Excitatory Neurons. A heat map of selected gene expression data from RNA-seq performed on undifferentiated iPSCs, Quick-Neuron™ Excitatory Neurons (EX only) cultured for 10 days and 38 days, Quick-Neuron™ Excitatory Neurons cocultured with primary astrocytes (EX+AST) for 18 and 52 days, and primary fetal and adult brain samples is shown. Values represent log10(TPM + 1). Data courtesy of Ricoh.

Principal Component Analysis (PCA)

Principal Component Analysis (PCA)

Quick-Neuron™ Excitatory Neurons display gene expression profiles similar to those of human brain: RNA-seq was performed on undifferentiated iPSCs, Quick-Neuron™Excitatory Neurons (EX only) cultured for 10 days and 38 days, Excitatory neurons cocultured with primary astrocytes (EX+AST) for 18 and 52 days, and primary fetal and adult brain samples. Principal component analysis indicates that Quick-Neuron™ Excitatory Neurons display gene expression similar to that of the human brain, particularly when grown with astrocytes. As cells remain in culture over time they more closely resemble adult human brain cells. Data courtesy of Ricoh.

Product Specifications

ParametersSpecifications
Product NameQuick-Neuron™ Excitatory - SeV Kit
Catalog No.EX-SeV
Product ComponentsQN-SeV-P (undiluted), Component N, Component G1, Component G2, and Component P
Storage ConditionsSeV should be stored at -80°C. All other components can be stored at -20°C or -80°C.
Cell TypeExcitatory Neurons
Induction MethodTranscription factors delivered by Sendai virus
DifferentiationAt day 7 post-differentiation (CW50065)
>80% TUBB3+,
>50% VGLUT1+/TUBB3+
SterilityNo growth observed
MycoplasmaNo DNA detected
Restricted UseFor Research Use Only. Not for use in diagnostic or therapeutic procedures.

Resources

Patient-Derived iPSC Neuronal Models Reveal Alzheimer’s Disease-Associated Pathology and Provide a Platform for Drug Discovery (SfN 2025)

Build Disease Models That Matter: The Power of Custom iPSC Differentiation

Long-Term Functional Characterization of Human iPSC-Derived Excitatory Neurons with High-Density Multielectrode Arrays

Unlocking the Secrets of Alzheimer’s, Epilepsy, and More with Cutting-Edge iPSC Technology

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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.

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