For research use only
| Cat No. | ABC-SC2055 |
| Product Type | Human iPSCs |
| Cell Type | Induced Pluripotent Stem Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Fibroblast |
| Disease | Tuberous Sclerosis 2 |
| Storage | Liquid Nitrogen |
Cell Type: iPSC; Disease: Tuberous Sclerosis 2; TSC2 TSC2 GENE; TSC2.
HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2 is a disease-specific human induced pluripotent stem cell line derived from dermal fibroblasts of a donor diagnosed with Tuberous Sclerosis Complex (TSC) Type 2, an autosomal dominant disorder caused by mutations in the TSC2 gene. The resulting iPSCs (induced pluripotent stem cells) exhibit adherent growth with a high nucleus-to-cytoplasm ratio. They sustain pluripotency and reflect TSC2-related physiological traits. These cells retain the fundamental capacity for trilineage differentiation into ectoderm, mesoderm, and endoderm derivatives under directed conditions. They express core pluripotency marker SSEA-4. 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 Fibroblast-Tuberous Sclerosis 2, HighQC™ hiPSC TSC2, hiPSC-TSC2, HighQC™ Human Induced Pluripotent Stem Cells From Fibroblast-Tuberous Sclerosis Complex 2 |
| Species | Human |
| Cat.No | ABC-SC2055 |
| 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 | Fibroblast |
| Disease | Tuberous Sclerosis 2 |
| Storage | Liquid Nitrogen |
| Product Type | Human iPSCs |
| Gene Info | Gene: TSC2; Mutation: ARG1743GLN |
HighQC™ Human IPSC From Fibroblast-Tuberous Sclerosis 2 serves as a human in vitro model for developmental and mechanistic studies of tuberous sclerosis. Its pluripotent capacity enables differentiation into disease-relevant lineages, such as neural progenitors and astrocytes, to investigate mTOR pathway dysregulation and cortical tuber formation. This system supports the generation of brain organoids for neurodevelopmental disease modeling and provides a platform for compound screening aimed at identifying potential mTOR inhibitors.
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).