axoCells Human iPSC-Derived Neural Stem Cells - Alzheimer's Disease Patient (PSEN1 L286V) female donor
Specifications | |
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Product Category: | iPSC-Derived Cells |
Research Area: | Neuroscience |
Culture Properties: | Adherent |
Donor Age: | 38 years |
Donor Gender: | Female |
Donor Ethnicity: | Caucasian |
Pathology: | Alzheimer’s Disease |
Reprogramming Method: | Episomal vector |
Product Description
ax0112 Neural Stem Cells are derived from iPSCs generated from a 38-year-old female donor's dermal fibroblasts. They can be further differentiated to generate cortical excitatory neurons or striatal neurons.
- Express the typical markers of cerebral cortical neural stem cells (PAX6, FOXG1 and nestin)
- Spontaneously form polarized neural tube-like rosette structures when plated as a monolayer in culture
- Can be differentiated into high-quality cortical excitatory neurons and striatal neurons
The donor exhibited Alzheimer's symptoms at age 39 and has the PSEN1 L286V genotype. axoCells human iPSC-Derived Neural Stem Cells (NSCs) are derived from integration-free, episomally reprogrammed, induced pluripotent stem cells (iPSCs) under fully defined neural induction conditions. axoCells NSCs are easy to differentiate to neurons or mixed neural cell types, following our protocols and using our tailored media and reagent bundles.
We provide Neural Maintenance Medium, BDNF and GDNF growth factors and NeurOne supplements to drive differentiation to cortical excitatory neurons, as well as Neural Plating Medium and optimized SureBond-XF coating, all as individual reagents or in kit format with the cells.
Our cortical excitatory neurons have been specifically developed for use in mono-, co- and tri-culture models of neurodegenerative disease and for drug discovery with microglia, astrocytes and inhibitory interneurons (ax0662 or ax0667).
The NSCs express typical markers of cerebral cortical neural stem and progenitor cells such as PAX6, FOXG1 and nestin, and spontaneously form polarized neural tube-like rosette structures when plated as a monolayer in culture. Additionally, axoCells NSCs are capable of generating a spectrum of cerebral cortical excitatory and striatal neurons that are electrically active and have the ability to form functional synapses and circuits in vitro. After thawing and plating, the neural stem cells terminally differentiate to acquire mature electrophysiological properties, and form functional synaptic networks over a period of ~ 20 days. Neurons derived from axoCells NSCs can be maintained in culture long-term (>1 year).
Supporting Data
Limited License Terms
Axol Bioscience's Limited License TermsGenetically Modified Organism (GVO)
See General Terms.
Product Citations
- Xiong J, Kang SS, Wang M, Wang Z, Xia Y, Liao J, Liu X, Yu SP, Zhang Z, Ryu V, Yuen T, Zaidi M, Ye K. (2023) FSH and ApoE4 contribute to Alzheimer's disease-like pathogenesis via C/EBPβ/δ-secretase in female mice Nature Communications
- Chen G, Kang SS, Wang Z, Ahn EH, Xia Y, Liu X, Sandoval IM, Manfredsson FP, Zhang Z, Ye K. (2021) Netrin-1 receptor UNC5C cleavage by active δ-secretase enhances neurodegeneration, promoting Alzheimer's disease pathologies.
- Xia Y, Wang ZH, Zhang J, Liu X, Yu SP, Ye KX, Wang JZ, Ye K, Wang XC. (2020) C/EBPβ is a key transcription factor for APOE and preferentially mediates ApoE4 expression in Alzheimer's disease Molecular Psychiatry
- Zollo A, Allen Z, Rasmussen HF, Iannuzzi F, Shi Y, Larsen A, Maier TJ, Matrone C. (2017) Sortilin-Related Receptor Expression in Human Neural Stem Cells Derived from Alzheimer's Disease Patients Carrying the APOE Epsilon 4 Allele Neural Plasticity
- Catalog Number
ax0112-GVO-AX - Supplier
Axol Bioscience - Size
- Shipping
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