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For Research Use Only. Not For Clinical Use.

STEMOD™ iPSC-derived ALS Disease Model (SOD1, D90A)(MoCNS-WQ024)

Datasheet

ALS is a severe neurodegenerative condition characterized by loss of motor neurons in the spinal cord and brain. This disease cell model has a D90A mutation in SOD1 gene. Generating pluripotent stem cells from fibroblasts, then differentiate into motor neurons . This disease cell model provides a platform to explore disease mechanisms in ALS.

Specifications
Organ System Central Nervous System
Disease Amyotrophic Lateral Sclerosis (ALS)
Target Gene SOD1
Gene Function The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body.
Mutation D90A
Phenotype Neurite swelling appeared early in spinal MNs, but rarely in non-MNs
Source Fibroblasts
Cellular Assays Immunocytochemistry, RT-PCR, , Western Blotting, Genotyping, Allelic Imbalance Assay, ELISA and Electrophysiology
Target Gene
Gene ID 6647
Uniprot ID P00441

For Research Use Only. Not For Clinical Use.

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