For research use only
| Cat No. | ABC-SC255Y |
| Product Type | Motor Neurons |
| Cell Type | Neural/Glial Cells |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Central Nervous System |
| Disease | ALS; Frontotemporal Dementia |
| Storage | Liquid Nitrogen |
HighQC Human iPSC-Derived Motor Neurons SOD1 G93A/G93A model ALS-linked motor neuron degeneration for SOD1-associated neurodegenerative CNS research.
HighQC Human iPSC-Derived Motor Neurons SOD1 G93A/G93A are human iPSC-derived motor neurons generated from a human iPSC line originally derived from adult skin fibroblasts. These cryopreserved cells provide a defined in vitro model for amyotrophic lateral sclerosis (ALS) research and SOD1-associated neurodegenerative disease studies. The cells are produced through deterministic cell programming to support reproducible lineage-specific experimental systems. This line carries a homozygous SOD1 G93A missense mutation on both alleles, modeling SOD1 protein misfolding relevant to familial ALS, without implying a fixed clinical phenotype. They retain neuronal lineage characteristics associated with motor neuron models. Quality control testing includes sterility assessment and lineage characterization by protein expression and gene expression assays, where applicable. Each lot undergoes rigorous screening and isolation procedures, and is rigorously tested to ensure it is free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | Motor Neurons SOD1 G93A/G93A; HighQC Human iPSC-Derived Motor Neurons SOD1 G93A/G93A; SOD1 |
| Species | Human |
| Cat.No | ABC-SC255Y |
| Product Category | Stem Cells |
| Size/Quantity | 1 vial |
| Cell Type | Neural/Glial Cells |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Central Nervous System |
| Disease | ALS; Frontotemporal Dementia |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Motor Neurons |
| Quality Control | All cells test negative for mycoplasma, bacteria, yeast, and fungi. |
HighQC Human iPSC-Derived Motor Neurons SOD1 G93A/G93A are intended for research use in controlled in vitro workflows. They can be used for disease-relevant mechanism studies, genotype-associated pathway analysis, target validation, and candidate therapeutic evaluation in a human iPSC-derived motor neuron model. As a homozygous SOD1 misfolding model, this line supports studies of SOD1 protein aggregation and motor neuron toxicity relevant to familial ALS, at the mechanism and assay-development level, not clinical or diagnostic use.