For research use only
| Cat No. | ABC-SC0211 |
| Product Type | Human iPSCs |
| Cell Type | Induced Pluripotent Stem Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Disease | Amyotrophic Lateral Sclerosis |
| Storage | Liquid Nitrogen |
Amyotrophic Lateral Sclerosis, female donor, Primary cell type: Fibroblast
HighQC™ human induced pluripotent stem cells derived from skin fibroblasts of patients with amyotrophic lateral sclerosis (ALS). These cells exhibit a high nuclear-to-cytoplasmic ratio with prominent nucleoli and grow as compact colonies under feeder-free, adherent conditions. These cells are generated by transducing OCT4, SOX2, KLF4, and c-MYC into patient-derived skin fibroblasts using Sendai virus. They express pluripotency markers including OCT4, SSEA4. These cells exhibit self-renewal capacity and retain the full pluripotent differentiation potential into all three germ layers—ectoderm, mesoderm, and endoderm under directed differentiation protocols. 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 | HighQC™ Human Induced Pluripotent Stem Cells, From Amyotrophic Lateral Sclerosis, Human iPSC-ALS, hIPSC-ALS, Human Induced Pluripotent Stem Cells ALS |
| Species | Human |
| Cat.No | ABC-SC0211 |
| Product Category | Stem Cells |
| Size/Quantity | 1 vial |
| Cell Type | Induced Pluripotent Stem Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Disease | Amyotrophic Lateral Sclerosis |
| Biosafety Level | 1 |
| Storage | Liquid Nitrogen |
| Product Type | Human iPSCs |
HighQC™ Human Induced Pluripotent Stem Cells, From Amyotrophic Lateral Sclerosis serve as a powerful tool for advancing research into neurodegenerative diseases. These patient-specific cells can be differentiated into motor neurons, astrocytes, and other central nervous system cell types, enabling detailed modeling of Amyotrophic Lateral Sclerosis (ALS) pathology in vitro. These cells represent an ALS patient-derived iPSC line, supporting disease-specific modeling and mechanistic studies of amyotrophic lateral sclerosis.
When you publish your research, please cite our product as "AcceGen Biotech Cat.# XXX-0000". In return, we’ll give you a $200 coupon. Simply click here and submit your paper’s PubMed ID (PMID).