For research use only
| Cat No. | ABC-SC0028T |
| Product Type | Human Mesenchymal Stem Cells |
| Cell Type | Mesenchymal Stem Cell |
| Species | Human |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Bone Marrow |
| Disease | Muscular Dystrophy |
| Storage | Liquid Nitrogen |
HighQC™ Human Bone Marrow Derived Mesenchymal Stem Cell/Muscular Dystrophy Patient for muscular dystrophy modeling and regenerative therapy research.
HighQC™ Human Bone Marrow Derived Mesenchymal Stem Cells (BM-MSCs) / Muscular Dystrophy (MD) Patient are primary mesenchymal stem cells isolated from bone marrow aspirates of donors with Duchenne Muscular Dystrophy (DMD). They express the specific markers of mesenchymal lineage, including CD73, CD90, and CD105, confirming their lineage identity. MD patient-derived BM-MSCs often exhibit morphological alterations and cellular dysfunction, such as impaired proliferation, differentiation defects, and increased senescence, which reflect disease-associated dysfunction. These cells provide a valuable model to investigate the molecular pathology of muscular dystrophies. 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 Bone Marrow Derived Mesenchymal Stem Cell/ Muscular Dystrophy Patient, Human BM-MSC-MD, hBM-MSC-MD, Human Bone Marrow MSC Muscular Dystrophy |
| Species | Human |
| Cat.No | ABC-SC0028T |
| Product Category | Stem Cells |
| Size/Quantity | 1 vial |
| Cell Type | Mesenchymal Stem Cell |
| Growth Mode | Adherent |
| Shipping Info | Dry Ice |
| Growth Conditions | 37 ℃, 5% CO2 |
| Source Organ | Bone Marrow |
| Disease | Muscular Dystrophy |
| Storage | Liquid Nitrogen |
| Product Type | Human Mesenchymal Stem Cells |
HighQC™ Human Bone Marrow Derived Mesenchymal Stem Cells / Muscular Dystrophy Patient are employed in preclinical and translational research targeting Duchenne Muscular Dystrophy (DMD). They can be applied in cellular therapy strategies aiming at restoring dystrophin expression in skeletal and cardiac muscle through donor cell engraftment and myogenic differentiation, contributing to improved muscle histology and function in preclinical and early clinical evaluations.
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).