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

Quick-Neuron™ human iPSC-derived cholinergic neurons are off-the-shelf neurons that provide a consistent, biologically relevant in vitro model of human cholinergic neuronal function. These cryopreserved, ready-to-use iPSC-derived neurons mature rapidly in culture and deliver reproducible performance for studying cholinergic signaling, synaptic activity, neuronal network development, neurodegenerative disease research, drug discovery, and neurotoxicity screening.

SKU: CH-SeV-HC-CW50065 Categories: , ,

$850.00

Advantages of iPSC-Derived Cholinergic Neurons

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

Cholinergic Neuron 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.

cholinergic neuron protocol
cholinergic neurons phase contrast

Cholinergic neuron morphology is confirmed via phase contrast imagery: Representative phase contrast images of Quick-Neuron™ Cholinergic – Human iPSC-derived Neurons on days 1-3 post-thaw. (scale bar = 100 μm)

Cholinergic Neuron Characterization

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

Cholinergic Neuron Marker Expression

Understanding the role of cholinergic 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.
CH SeV ICC Merge

Merge

CH SeV ICC TUBB3

TUBB3

CH SeV ICC ChAT

ChAT

CH SeV ICC Nuclei

Nuclei

iPSC-derived cholinergic neurons express neuronal markers and display typical neurite growth. Immunofluorescent staining of Quick-Neuron™ Cholinergic – Human iPSC-derived Neurons on Day 3 post-thaw that shows expression of the pan-neuronal marker TUBB3 and the cholinergic neuron marker ChAT.

Additional Cholinergic Neuron Data

ALS Disease Study

CH SeV ALS Study Healthy Control

Healthy Control

74 yr, Female, Caucasian

CH SeV ALS Study ALS Patient

ALS Patient

62 yr, Female, Caucasian

ALS Disease Study: Healthy control and ALS patient-derived iPSCs were differentiated into cholinergic neurons. The cells were fixed at day 10 from iPSCs and stained by TUBB3 (Green) and TDP-43 (Red).

Neurite Length Analysis

cholinergic neuron neurite length analysis

Neurite Length Analysis: Our fast differentiation enables quick and quantitative comparison between healthy and patient or treated and non-treated cultures.

Product Specifications

Parameters Specifications
Product Name Quick-Neuron™ Cholinergic - Human iPSC-Derived Neurons
Catalog No. CH-SeV-HC-CW50065
Product Components Cryopreserved cells, Component N1, Component A, and Component P
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 Cholinergic 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 Sendai virus
Growth Properties Adherent
Number of viable cells > 1.0 million viable cells per vial upon thawing
Cell viability and remaining live cells >70% at day 1, >211 live cells per mm2
>50% at day 7, >211 live cells per mm2
Differentiation >80% TUBB3 positive cells
>50% ChAT positive cells among TUBB3 positive cells
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.

Cholinergic Neuron Resources

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

Protective effects of NAMPT or MAPK inhibitors and NaR on Wallerian degeneration of mammalian axons

Tools to Study Neurodegeneration: iPSC-derived Neurons, Nerve Organoids, and Synaptogenic Beads

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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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