For research use only
| Cat No. | ABC-SC2089 |
| Product Type | Human iPSCs |
| Cell Type | Induced Pluripotent Stem Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | PBMC |
| Disease | Primary Lateral Sclerosis |
| Storage | Liquid Nitrogen |
Advance HighQC™ Human IPSC From PBMC-Primary Lateral Sclerosis for neurodegenerative disease modeling, therapeutic screening, and regenerative studies.
HighQC™ Human IPSC From PBMC-Primary Lateral Sclerosis is a disease-specific human induced pluripotent stem cell (iPSC) line derived from peripheral blood mononuclear cells (PBMCs) of a donor diagnosed with Primary Lateral Sclerosis (PLS). The reprogramming was performed using non-integrating episomal plasmid method. The resulting iPSCs (induced pluripotent stem cells) exhibit adherent growth with a high nucleus-to-cytoplasm ratio and well-defined borders. The cells sustain pluripotency for PLS-related neural pathway mechanism studies. They retain the fundamental capacity for trilineage differentiation into cell types of all three germ layers (ectoderm, mesoderm, and endoderm). 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 PBMC-Primary Lateral Sclerosis, HighQC™ hiPSC PLS, hiPSC-PLS, HighQC™ Human Induced Pluripotent Stem Cells From Peripheral Blood Mononuclear Cells-Primary Lateral Sclerosis |
| Species | Human |
| Cat.No | ABC-SC2089 |
| 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 | PBMC |
| Disease | Primary Lateral Sclerosis |
| Storage | Liquid Nitrogen |
| Product Type | Human iPSCs |
HighQC™ Human IPSC From PBMC-Primary Lateral Sclerosis provides a patient-specific model for studying this upper motor neuron disorder. Its pluripotent capacity enables directed differentiation into cortical motor neurons, facilitating research on selective neuronal vulnerability and disease mechanisms. This system supports the generation of neural circuit models to investigate corticospinal tract pathology and serves as a platform for compound screening in relevant cellular assays.
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).