For research use only
| Cat No. | ABC-SC2088 |
| Product Type | Human iPSCs |
| Cell Type | Induced Pluripotent Stem Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | LCL |
| Disease | Amyotrophic Lateral Sclerosis |
| Storage | Liquid Nitrogen |
Cell Type iPSC Primary Tissue LCL Reprogramming Method Episomal Plasmid Disease ALS.
HighQC™ Human IPSC From LCL-ALS is a disease-specific human induced pluripotent stem cell line generated by reprogramming a lymphoblastoid cell line (LCL), which was originally derived from the peripheral blood mononuclear cells (PBMCs) of a donor diagnosed with Amyotrophic Lateral Sclerosis (ALS). The reprogramming was performed using non-integrating episomal plasmid method. The resulting human iPSCs (induced pluripotent stem cells) exhibit adherent growth with well-defined borders and a high nucleus-to-cytoplasm ratio. They maintain pluripotency for ALS-related neural mechanism research. These cells retain the fundamental capacity for trilineage differentiation into cell types of the ectoderm, mesoderm, and endoderm germ layers. Core pluripotency marker SSEA-4 is expressed. The cells undergo rigorous screening and isolation procedures, and are rigorously tested to ensure they are free of contamination from HIV-1, HBV, HCV, Syphilis, Mycoplasma, Fungi, Yeast, and Bacteria.
| Product Code | HighQC™ Human IPSC From LCL-ALS, HighQC™ hiPSC ALS LCL, hiPSC-ALS-LCL, HighQC™ Human Induced Pluripotent Stem Cells From Lymphoblastoid Cell Line-Amyotrophic Lateral Sclerosis |
| Species | Human |
| Cat.No | ABC-SC2088 |
| 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 |
| Source Organ | LCL |
| Disease | Amyotrophic Lateral Sclerosis |
| Storage | Liquid Nitrogen |
| Product Type | Human iPSCs |
HighQC™ Human IPSC From LCL-ALS provides a genetically relevant model for motor neuron disease research. Its pluripotent capacity enables directed differentiation into motor neurons, facilitating studies on neurodegeneration, excitotoxicity, and protein aggregation mechanisms. This system supports the development of neural organoids for disease modeling and serves as a platform for high-content drug screening to identify neuroprotective candidates.
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).